NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0472-0380
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Phosphoric Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) E4GA8884NN.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7664-38-2 and the RxNorm Concept ID (RxCUI) 8259. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
PHOSPHORIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
E4GA8884NN
The specific atomic composition represented as a molecular structure string.
InChIKey
H3O4P International Chemical Identifier digital signature for unique molecular identification.
SMILES String
NBIIXXVUZAFLBC-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
OP(=O)(O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Phosphoric Acid. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
PHOSPHORIC ACID
OF
Common Names & Synonyms
ACIDUM PHOSPHORICUM
CN
AMBERPHOS 54
CN
ETIDRONATE DISODIUM IMPURITY A [EP IMPURITY]
CN
PAMIDRONATE DISODIUM PENTAHYDRATE IMPURITY B [EP IMPURITY]
CN
PHOSPHORIC ACID [FCC]
CN
PHOSPHORIC ACID [FHFI]
CN
PHOSPHORIC ACID [HSDB]
CN
PHOSPHORIC ACID [II]
CN
PHOSPHORIC ACID [MART.]
CN
PHOSPHORIC ACID [MI]
CN
PHOSPHORIC ACID [ORANGE BOOK]
CN
PHOSPHORIC ACID [USP-RS]
CN
PHOSPHORIC ACID [VANDF]
CN
PHOSPHORIC ACID [WHO-DD]
CN
PHOSPHORICUM ACIDUM
CN
PHOSPHORICUM ACIDUM [HPUS]
CN
VOCOCID
CN
WC-REINIGER
CN
ZOLEDRONIC ACID MONOHYDRATE IMPURITY F [EP IMPURITY]
CN
Systematic Nomenclature
ORTHOPHOSPHORIC ACID
SYS
Technical Codes
E 338
CD
E-338
CD
FEMA NO. 2900
CD
INS NO.338
CD
INS-338
CD
NSC-80804
CD
Y-11A06
CD
NDC Products Containing PHOSPHORIC ACID
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
Actavis Pharma, Inc.
Active Listing
Alcon Laboratories, Inc.
NDC Product
Human Prescription DrugPhenylephrine Hydrochloride NDC 0065-0343
- Generic Name
- Phenylephrine Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPhenylephrine Hydrochloride NDC 0065-0349
- Generic Name
- Phenylephrine Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
American Sales Company
NDC Product
Human Otc DrugChildrens Loratadine Sugar Free NDC 41520-131
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Astellas Pharma US, Inc.
NDC Product
Human Prescription DrugVyloy NDC 0469-3425
- Generic Name
- Zolbetuximab
- Dosage Form
- Injection, Powder, For Suspension
- Route
- Intravenous
- Marketing
- BLA
Active Listing
Atlantic Biologicals
NDC Product
Human Otc DrugChildrens Loratadine Oral NDC 17856-6767
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugAlka-seltzer Extra Strength Heartburn Reliefchews NDC 0280-0042
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Reliefchews NDC 0280-0221
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Reliefchews Strawberry And Orange NDC 0280-0224
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugClaritin Allergy NDC 11523-0101
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugChildren Claritin Allergy NDC 11523-4360
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
Becton Dickinson and Company
NDC Product
Human Otc DrugBd E-z Scrub NDC 17271-205
- Generic Name
- Povidone-iodine
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Better Living Brands LLC
NDC Product
Human Otc DrugLoratadine NDC 21130-042
- Generic Name
- Loratadine Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Biomedical Research Foundation of Northwest Louisiana
NDC Product
Human Prescription DrugFludeoxyglucose F18 NDC 24562-003
- Generic Name
- Fludeoxyglucose F-18
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
Boiron
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-3993
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-3994
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4000
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4007
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4008
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4009
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4010
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4011
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 0220-4012
- Generic Name
- Phosphoric Acid
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Burkhart Dental Supply Inc
NDC Product
Human Prescription DrugBurkhart NDC 43498-100
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugBurkhart NDC 43498-101
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugBurkhart NDC 43498-102
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugBurkhart NDC 43498-103
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
COLGATE PALMOLIVE COMPANY
NDC Product
Human Otc DrugColgate Optic White Advanced Sparkling White NDC 35000-978
- Generic Name
- Sodium Monofluorophosphate
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-952
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-953
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-954
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-955
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chattem, Inc.
NDC Product
Human Otc DrugDulcolax Chewy Bites Assorted Fruits NDC 41167-0256
- Generic Name
- Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDulcolax Chewy Fruit Bites Cherry Berry NDC 41167-0257
- Generic Name
- Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugOrajel Antiseptic Rinse For All Mouth Sores NDC 10237-760
- Generic Name
- Hydrogen Peroxide And Menthol
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel Antiseptic Alcohol-free Mouth Sore Rinse NDC 10237-784
- Generic Name
- Hydrogen Peroxide, Menthol
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 2x Gum Pain Alcohol-free NDC 10237-799
- Generic Name
- Menthol And Hydrogen Peroxide
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Colgate Oral Pharmaceuticals, Inc.
NDC Product
Human Otc Drug- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Colgate-Palmolive - do not use
NDC Product
Human Otc DrugColgate Enamel Strength Mouthwash NDC 35000-734
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Colgate-Palmolive Company
NDC Product
Human Otc DrugColgate Kids Unicorn Alcohol Free NDC 35000-334
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTp Col Ow Purple NDC 35000-419
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugColgate Kids Minions Mouthwash NDC 35000-727
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOptic White Non-hp Stain Fighter Clean Mint NDC 35000-793
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugColgate Optic White Purple NDC 35000-796
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugColgate Optic White Non-hp Stain Fighter Fresh Mint NDC 35000-797
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugColgate Optic White Charcoal NDC 35000-798
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugColgate Optic White Relief NDC 35000-799
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugColgate Optic White Stain Fighter Sens Relief NDC 35000-998
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTp Ow Stainfighter Clean Mint NDC 35000-999
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Cosette Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0713-0326
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0713-0327
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMometasone Furoate NDC 0713-0634
- Generic Name
- Mometasone Furoate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMometasone Furoate NDC 0713-0635
- Generic Name
- Mometasone Furoate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0713-0659
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Crosstex International Inc.
NDC Product
Human Prescription DrugZap Apf NDC 24794-100
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-101
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-102
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-103
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-104
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-105
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-106
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-107
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Neutral NDC 24794-108
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugZap Apf NDC 24794-109
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAlclometasone Dipropionate NDC 0168-0263
- Generic Name
- Alclometasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0168-0033
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0168-0040
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0168-0041
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0168-0055
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0168-0056
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0168-0057
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0168-0267
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Lotion, Augmented
- Route
- Topical
- Marketing
- ANDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugHumatrope NDC 0002-8147
- Generic Name
- Somatropin
- Dosage Form
- Kit
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumatrope NDC 0002-8148
- Generic Name
- Somatropin
- Dosage Form
- Kit
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumatrope NDC 0002-8149
- Generic Name
- Somatropin
- Dosage Form
- Kit
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
Encube Ethicals, Inc.
NDC Product
Human Prescription DrugClindamycin And Benzoyl Peroxide NDC 21922-068
- Generic Name
- Clindamycin And Benzoyl Peroxide
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMometasone Furoate NDC 21922-071
- Generic Name
- Mometasone Furoate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 21922-104
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Lotion, Augmented
- Route
- Topical
- Marketing
- ANDA
Active Listing
Gingi-Pak a Division of the Belport
NDC Product
Human Otc DrugPerio Armor NDC 10129-018
- Generic Name
- 1.7% Hydrogen Peroxide
- Dosage Form
- Gel
- Route
- Dental; Periodontal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugPerio Armor NDC 10129-019
- Generic Name
- 1.7% Hydrogen Peroxide
- Dosage Form
- Gel
- Route
- Dental; Periodontal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Guna spa
NDC Product
Human Otc DrugGuna-mood NDC 17089-265
- Generic Name
- 5-hydroxy Tryptophan,dl - Alfalfa - Avena Sativa Flowering T...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
H E B
NDC Product
Human Otc DrugOral Sore Antiseptic NDC 37808-024
- Generic Name
- Hydrogen Peroxide, Menthol
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 37808-119
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Loratadine Sugar Free NDC 37808-131
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAnticavity Fluoride Rinse NDC 37808-163
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 37808-435
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol Free Refreshing Mint NDC 37808-576
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol-free Anticavity NDC 37808-942
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
HEB
NDC Product
Human Otc DrugHeb Anti Nausea NDC 37808-883
- Generic Name
- Dextrose(glucose),levulose(fructose),phosphoric Acid
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Hahnemann Laboratories, INC.
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3439
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3440
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3441
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3442
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3443
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3444
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3445
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3446
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugAcidum Phosphoricum NDC 37662-3447
- Generic Name
- Acidum Phosphoricum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0118
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0119
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0183
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Berry Shake NDC 0135-0184
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Tropical Fruit Smoothie NDC 0135-0185
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Raspberry Lemonade NDC 0135-0188
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0606
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0618
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Peppermint NDC 0135-0623
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites With Gas Relief NDC 0135-0624
- Generic Name
- Calcium Carbonate And Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Mixed Fruit NDC 0135-0641
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Orange And Cream Es NDC 0135-0642
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugVecuronium Bromide NDC 0143-9232
- Generic Name
- Vecuronium Bromide
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVecuronium Bromide NDC 0143-9234
- Generic Name
- Vecuronium Bromide
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCladribine NDC 0143-9871
- Generic Name
- Cladribine
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
Hisun Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugCladribine NDC 42658-010
- Generic Name
- Cladribine
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCladribine NDC 42658-010
- Generic Name
- Cladribine
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc DrugLoratadine NDC 30142-062
- Generic Name
- Loratadine Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugKroger Anti Nausea Cherry Flavor NDC 30142-708
- Generic Name
- Dextrose(glucose),levulose(fructose),phosphoric Acid
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Kroger Company
NDC Product
Human Otc DrugChildrens Allergy Relief NDC 30142-723
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-0671
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-1719
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lupin Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 43386-570
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 43386-571
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 43386-572
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoclopramide Hydrochloride NDC 43386-580
- Generic Name
- Metoclopramide Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoclopramide Hydrochloride NDC 43386-581
- Generic Name
- Metoclopramide Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 43386-930
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 43386-931
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
MEIJER DISTRIBUTION, INC.
NDC Product
Human Otc DrugMeijer Anti Nausea NDC 41250-495
- Generic Name
- Dextrose(glucose),levulose(fructose),phosphoric Acid
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Major Pharmaceuticals
NDC Product
Human Otc DrugChildrens Loratadine Oral NDC 0904-6767
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Meijer, Inc.
NDC Product
Human Otc DrugAlcohol-free Anticavity NDC 41250-482
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOral Antivavity NDC 41250-576
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Allergy Relief NDC 41250-716
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 41250-971
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NORTHSTAR RX LLC
NDC Product
Human Prescription DrugClotrimazole And Betamethasone Dipropionate NDC 16714-496
- Generic Name
- Clotrimazole And Betamethasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Natural Creations, Inc
NDC Product
Human Otc DrugVitality Female NDC 43406-0605
- Generic Name
- Aralia Quinquefolia, Avena Sativa, Berberis Vulgaris, Causti...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMood NDC 43406-0680
- Generic Name
- Aralia Quin, Cimicifuga, Spigelia Anth, Arg Nit, Arsenicum A...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPanacode NDC 43406-0686
- Generic Name
- Syzygium, Hydrastis, Adrenalinum, Pancreatinum, Pituitarum P...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGastrozen NDC 43406-0690
- Generic Name
- Coffea Tosta, Glycyrrhiza, Phytolacca, Taraxacum, Hydrastis,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Natural Creations, Inc.
NDC Product
Human Otc DrugViral Hp NDC 43406-0052
- Generic Name
- Arsenic Trioxide, Atropa Belladonna, Echinacea Angustifolia,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugWeight Management Hp NDC 43406-0053
- Generic Name
- Arsenic Trioxide, Gold, Oyster Shell Calcium Carbonate, Crud...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugStress / Fatigue NDC 43406-0612
- Generic Name
- Epinephrine, Thyroid Unspecified,bos Taurus Pituitary Gland,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCandida Hp NDC 43406-0672
- Generic Name
- Baptisia Tinctoria Root, Echinacea Purpurea, Glycyrrhiza Gla...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugStress / Fatigue NDC 43406-0695
- Generic Name
- Adrenalinum, Pituitarum Gland, Thyroidinum, Arsenicum Alb, C...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugLeqvio NDC 0078-1000
- Generic Name
- Inclisiran
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- NDA
Active Listing
Patrin Pharma, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hcl NDC 39328-054
- Generic Name
- Methylphenidate Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hcl NDC 39328-154
- Generic Name
- Methylphenidate Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
RUGBY LABORATORIES
NDC Product
Human Otc DrugAnti Nausea NDC 0536-1302
- Generic Name
- Dextrose(glucose),levulose(fructose),phosphoric Acid
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugChildrens Allergy Relief NDC 11822-0620
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOral Sore Antiseptic NDC 11822-3024
- Generic Name
- Hydrogen Peroxide, Menthol
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 11822-9718
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
NDC Product
Human Otc DrugPhosphoricum Acidum NDC 15631-0335
- Generic Name
- Phosphoricum Acidum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPhosphoric Acid NDC 15631-2886
- Generic Name
- Phosphoric Acid
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Sagent Pharmaceuticals
NDC Product
Human Prescription DrugVecuronium Bromide NDC 25021-685
- Generic Name
- Vecuronium Bromide
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVecuronium Bromide NDC 25021-686
- Generic Name
- Vecuronium Bromide
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugEdaravone NDC 0781-3527
- Generic Name
- Edaravone
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
TOPCO ASSOCIATES LLC
NDC Product
Human Otc DrugAnti Nausea Liquid NDC 36800-708
- Generic Name
- Phosphorated Carbohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
TRP Company
NDC Product
Human Otc DrugChronic Fatigue Therapy NDC 17312-170
- Generic Name
- Epinephrine, Gold, Chelidonium Majus, Echinacea, Ginkgo, Hel...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatural Relief Diarrhea Relief NDC 17312-473
- Generic Name
- Aloe, Citrullus Colocynthis, Croton Tiglium, Lycopodium Clav...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Target Corporation
NDC Product
Human Otc DrugAnticavity Fluoride Rinse NDC 11673-163
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAntibiotic And Pain Relief NDC 11673-770
- Generic Name
- Neomycin Sulfate, Polymyxin B Sulfate, And Pramoxine Hydroch...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Kroger Co.
NDC Product
Human Otc DrugAnticavity NDC 30142-163
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol-free Anticavity NDC 30142-482
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOral Antivavity NDC 30142-576
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Procter & Gamble Manufacturing Company
NDC Product
Human Otc DrugKids Crest Bubblegum Rush NDC 37000-167
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCrest 3d White Luxe Diamond Strong NDC 37000-862
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCrest Pro-health Advanced W/extra Whitening NDC 37000-867
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Topco Associates LLC
NDC Product
Human Otc DrugMouth Rinse NDC 36800-001
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol-free Anticavity NDC 36800-482
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTopcare Childrens Allergy NDC 36800-608
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 36800-803
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 36800-971
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugMometasone Furoate NDC 13668-527
- Generic Name
- Mometasone Furoate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
Trigen Laboratories, LLC
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-700
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-706
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-707
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-708
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-709
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-710
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-711
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
United Natural Foods, Inc. dba UNFI
NDC Product
Human Otc DrugAnticavity NDC 41163-011
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEqualine Childrens Allergy Relief NDC 41163-633
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 41163-971
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Validus Pharmaceuticals LLC
NDC Product
Human Prescription DrugRaldesy Tm NDC 30698-455
- Generic Name
- Trazodone Hydrochloride Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAtoncy NDC 30698-456
- Generic Name
- Atomoxetine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
WALGREEN COMPANY
NDC Product
Human Otc DrugLoratadine NDC 0363-0771
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS CO.
NDC Product
Human Otc DrugWalgreen Anti Nausea Cherry Flavor NDC 0363-7080
- Generic Name
- Phosphorated Carbohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugWalgreen Children Anti Nausea NDC 0363-7081
- Generic Name
- Dextrose, Levulose, Phosphoric Acid
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Walgreen Co.
NDC Product
Human Otc DrugMouth Rinse NDC 0363-0163
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAnticavity NDC 0363-0171
- Generic Name
- Sodium Fluoride
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOral Sore Antiseptic NDC 0363-1045
- Generic Name
- Hydrogen Peroxide, Menthol
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugChildrens Walitin NDC 0363-2108
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Loratadine Sugar Free NDC 0363-2131
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens Company
NDC Product
Human Otc DrugWalgreens Kids Multi-antibiotic With Pain Relief Cream NDC 0363-2122
- Generic Name
- Polymyxin B Sulfate, Neomycin Sulfate, Pramoxine Hydrochlori...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Multi-antibiotic With Pain Relief Cream NDC 0363-2123
- Generic Name
- Polymyxin B Sulfate, Neomycin Sulfate, Pramoxine Hydrochlori...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
XGen Pharmaceuticals DJB, Inc.
NDC Product
Human Prescription DrugAmphotericin B NDC 39822-1055
- Generic Name
- Amphotericin B
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEdaravone NDC 39822-4500
- Generic Name
- Edaravone
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEdaravone NDC 39822-4510
- Generic Name
- Edaravone
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
