NDC Product
Human Prescription DrugOriahnn NDC 0074-1017
- Generic Name
- Elagolix And Estradiol And Norethisterone
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Alcohol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 3K9958V90M.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 64-17-5 and the RxNorm Concept ID (RxCUI) 448. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
ALCOHOL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
3K9958V90M
The specific atomic composition represented as a molecular structure string.
InChIKey
C2H6O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
OCC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Alcohol. 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
ALCOHOL
OF
ALCOHOL DENAT.
OF
Common Names & Synonyms
ALCOHOL [HSDB]
CN
ALCOHOL [II]
CN
ALCOHOL [MART.]
CN
ALCOHOL [ORANGE BOOK]
CN
ALCOHOL [USP-RS]
CN
ALCOHOL [VANDF]
CN
ALCOHOL [WHO-IP]
CN
ALCOHOL ANHYDROUS
CN
ALCOHOL DENATURED
CN
ALCOHOL DETERMINATION--ALCOHOL
CN
ALCOHOL, ABSOLUTE
CN
ALCOHOL, DEHYDRATED
CN
ALCOHOL, DEHYDRATED [II]
CN
ALCOHOL, DEHYDRATED [VANDF]
CN
ALCOHOL, DENATURED
CN
ALCOHOL, DENATURED [II]
CN
ALCOHOL, DENATURED [VANDF]
CN
ALCOHOL, DILUTED
CN
ALCOHOL, DILUTED [II]
CN
ALCOHOL,DEHYDRATED
CN
ALCOHOL,DEHYDRATED [VANDF]
CN
ALCOHOL,DENATURED
CN
ALCOHOL,DENATURED [VANDF]
CN
ALCOHOL,ETHYL
CN
ALCOHOL,ETHYL [VANDF]
CN
ALCOHOL,SDA [VANDF]
CN
ALCOHOLUM [WHO-IP LATIN]
CN
ANHYDROUS ETHANOL
CN
ANHYDROUS ETHANOL [JAN]
CN
AVAGARD COMPONENT ALCOHOL
CN
DEHYDRATED ALCOHOL
CN
DEHYDRATED ALCOHOL [USP MONOGRAPH]
CN
DEHYDRATED ALCOHOL [USP-RS]
CN
DEHYDRATED ETHANOL
CN
EDIBLE ALCOHOL
CN
ETHANOL [JAN]
CN
ETHANOL [WHO-DD]
CN
ETHANOL [WHO-IP]
CN
ETHANOL IN ALCOHOLIC BEVERAGES [IARC]
CN
ETHANOL, ANHYDROUS [EP MONOGRAPH]
CN
ETHANOL, DEHYDRATED
CN
ETHANOLUM [WHO-IP LATIN]
CN
ETHYL ALCOHOL & WATER
CN
ETHYL ALCOHOL [FCC]
CN
ETHYL ALCOHOL [FHFI]
CN
ETHYL ALCOHOL [MI]
CN
ETHYL ALCOHOL AND WATER
CN
ETHYL ALCOHOL, ABSOLUTE
CN
ETHYL ALCOHOL, DEHYDRATED
CN
ETHYLICUM
CN
ETHYLICUM [HPUS]
CN
GRAIN ALCOHOL
CN
HBN-1 COMPONENT ETHANOL
CN
SD ALCOHOL [VANDF]
CN
TECSOL
CN
VODKA
CN
VODKA [MI]
CN
Brand / Trade Names
ABLYSINOL
BN
Systematic Nomenclature
1-HYDROXYETHANE
SYS
ALCOHOL, ETHYL
SYS
ETHANOL
SYS
ETHYL ALCOHOL
SYS
ETHYL ALCOHOL (ETHANOL)
SYS
Technical Codes
B3324 [LANGUAL]
CD
FEMA NO. 2419
CD
NCI-C03134
CD
NSC-85228
CD
PM-6193-200
CD
NDC Products Containing ALCOHOL
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
AbbVie Inc.
Active Listing
NDC Product
Human Prescription DrugZemplar NDC 0074-1658
- Generic Name
- Paricalcitol
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGengraf NDC 0074-3108
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGengraf NDC 0074-3109
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNorvir NDC 0074-3399
- Generic Name
- Ritonavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKaletra NDC 0074-3956
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZemplar NDC 0074-4637
- Generic Name
- Paricalcitol
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKaletra NDC 0074-6799
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZemplar NDC 0074-9036
- Generic Name
- Paricalcitol
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZemplar NDC 0074-9037
- Generic Name
- Paricalcitol
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugTaytulla NDC 0023-5862
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol, And Ferrous Fum...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1277
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1278
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1279
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1280
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1281
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1282
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 0115-1324
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 0115-1325
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1479
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugNexium NDC 0186-4010
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4025
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4040
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4050
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-5020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-5040
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
BF ASCHER AND CO INC
NDC Product
Human Otc DrugItch X NDC 0225-0495
- Generic Name
- Benzyl Alcohol/pramoxine Hydrochloride
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
BOIRON
NDC Product
Human Otc DrugHemcalm NDC 0220-9178
- Generic Name
- Horse Chestnut, Collinsonia Canadensis Root, Hamamelis Virgi...
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Bausch Health US LLC
NDC Product
Human Prescription DrugJublia NDC 0187-5400
- Generic Name
- Efinaconazole
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
Bausch Health US, LLC
NDC Product
Human Prescription DrugMestinon NDC 0187-3010
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMestinon NDC 0187-3012
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMestinon NDC 0187-3013
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5170
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5172
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBenzamycin NDC 0187-5205
- Generic Name
- Erythromycin And Benzoyl Peroxide
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTargretin NDC 0187-5525
- Generic Name
- Bexarotene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
Boiron
NDC Product
Human Otc DrugColdcalm Kids NDC 0220-9060
- Generic Name
- Strychnos Nux-vomica Seed, Pulsatilla Vulgaris, Onion, Phyto...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare Arthritis NDC 0220-9077
- Generic Name
- Arnica Montana, Harpagophytum Procumbens Root, Harpagophytum...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare Bruise NDC 0220-9085
- Generic Name
- Arnica Montana
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCamilia Tummy NDC 0220-9099
- Generic Name
- Activated Charcoal, Matricaria Chamomilla, Copper, Citrullus...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCamilia Bedtime NDC 0220-9102
- Generic Name
- Matricaria Chamomilla, Arabica Coffee Bean, Phytolacca Ameri...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChestal Cold And Cough Honey NDC 0220-9121
- Generic Name
- Solanum Dulcamara Top, Ferrosoferric Phosphate, Goldenseal, ...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChestal Kids Cold And Cough Honey NDC 0220-9122
- Generic Name
- Solanum Dulcamara Top, Ferrosoferric Phosphate, Goldenseal, ...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugSleepcalm Kids NDC 0220-9309
- Generic Name
- Matricaria Chamomilla Whole, Gelsemium Sempervirens Root, Hy...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugThroatcalm NDC 0220-9329
- Generic Name
- Echinacea Angustifolia Whole, Plantago Major Whole
- Dosage Form
- Spray
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
NDC Product
Human Prescription DrugFluocinonide NDC 0168-0134
- Generic Name
- Fluocinonide
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
E.R. Squibb & Sons, L.L.C.
NDC Product
Human Prescription DrugReyataz NDC 0003-3622
- Generic Name
- Atazanavir
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3631
- Generic Name
- Atazanavir
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3638
- Generic Name
- Atazanavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugAmyvid NDC 0002-1200
- Generic Name
- Florbetapir F 18
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetevmo NDC 0002-2980
- Generic Name
- Selpercatinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetevmo NDC 0002-3977
- Generic Name
- Selpercatinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugCellcept NDC 0004-0261
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCellcept NDC 0004-0298
- Generic Name
- Mycophenolate Mofetil Hydrochloride
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
HIKMA PHARMACEUTICALS USA INC.
NDC Product
Human Prescription DrugEribulin Mesylate NDC 0143-9167
- Generic Name
- Eribulin Mesylate
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Pseudoephedrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
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 DrugTheraflu Expressmax Daytime Nighttime Value Pack NDC 0067-8125
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl And A...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8127
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8129
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8136
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8137
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Caplets NDC 0067-8145
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Tablet, Coated
- 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 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 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 DrugDigoxin NDC 0054-0057
- Generic Name
- Digoxin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCalcium Acetate NDC 0054-0088
- Generic Name
- Calcium Acetate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIcosapent Ethyl NDC 0054-0508
- Generic Name
- Icosapent Ethyl
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 0054-0742
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam Intensol NDC 0054-3185
- Generic Name
- Diazepam Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiphenoxylate Hydrochloride And Atropine Sulfate NDC 0054-3194
- Generic Name
- Diphenoxylate Hydrochloride And Atropine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-3555
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-3556
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone Intensol NDC 0054-3721
- Generic Name
- Prednisone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-3722
- Generic Name
- Prednisone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0054-3727
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0054-3730
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8724
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8739
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8740
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFulvestrant NDC 0143-9022
- Generic Name
- Fulvestrant
- Dosage Form
- Injection
- Route
- Intramuscular
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDihydroergotamine Mesylate NDC 0143-9151
- Generic Name
- Dihydroergotamine Mesylate
- Dosage Form
- Injection
- Route
- Intramuscular; Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDocetaxel NDC 0143-9204
- Generic Name
- Docetaxel
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDocetaxel NDC 0143-9205
- Generic Name
- Docetaxel
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDihydroergotamine Mesylate NDC 0143-9273
- Generic Name
- Dihydroergotamine Mesylate
- Dosage Form
- Injection
- Route
- Intramuscular; Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugArgatroban NDC 0143-9288
- Generic Name
- Argatroban
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEtoposide NDC 0143-9376
- Generic Name
- Etoposide
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugArgatroban NDC 0143-9377
- Generic Name
- Argatroban
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEtoposide NDC 0143-9510
- Generic Name
- Etoposide
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtoposide NDC 0143-9511
- Generic Name
- Etoposide
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtoposide NDC 0143-9512
- Generic Name
- Etoposide
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugArgatroban NDC 0143-9559
- Generic Name
- Argatroban
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArgatroban NDC 0143-9674
- Generic Name
- Argatroban
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDoxycycline Hyclate NDC 0143-9803
- Generic Name
- Doxycycline Hyclate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugDexamethasone Intensol NDC 0054-3176
- Generic Name
- Dexamethasone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-3177
- Generic Name
- Dexamethasone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8174
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8175
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8176
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8179
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
L Perrigo Company
NDC Product
Human Otc DrugMederma Pm NDC 0113-4124
- Generic Name
- Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Severe Nighttime NDC 0113-0019
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Time NDC 0113-0186
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-0294
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-0335
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nighttime NDC 0113-0459
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-1032
- Generic Name
- Minoxidil
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-1129
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMinoxidil NDC 0113-5129
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-6500
- Generic Name
- Minoxidil
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
Laboratoires Boiron
NDC Product
Human Otc DrugCalendula NDC 0220-1104
- Generic Name
- Calendula Officinalis Flowering Top
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare NDC 0220-9000
- Generic Name
- Arnica Montana
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare NDC 0220-9021
- Generic Name
- Arnica Montana
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare NDC 0220-9023
- Generic Name
- Arnica Montana
- Dosage Form
- Ointment
- Route
- Cutaneous
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare Value Pack NDC 0220-9042
- Generic Name
- Arnica Montana
- Dosage Form
- Kit
- Route
- Oral; Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnica Value Pack NDC 0220-9047
- Generic Name
- Arnica Montana
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare Bruise NDC 0220-9084
- Generic Name
- Arnica Montana
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugTemodar NDC 0085-1366
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1381
- Generic Name
- Temozolomide
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1417
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1425
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1430
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1519
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-3004
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Mission Pharmacal Company
NDC Product
Human Prescription DrugTexacort NDC 0178-0455
- Generic Name
- Hydrocortisone
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugSandimmune NDC 0078-0109
- Generic Name
- Cyclosporine
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSandimmune NDC 0078-0240
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSandimmune NDC 0078-0241
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRydapt NDC 0078-0698
- Generic Name
- Rydapt
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Prescription DrugDiphenhydramine Hydrochloride NDC 0121-0489
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0121-0653
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTrihexyphenidyl Hydrochloride NDC 0121-0658
- Generic Name
- Trihexyphenidyl Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0121-0678
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTheophylline NDC 0121-0820
- Generic Name
- Theophylline
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSulfamethoxazole And Trimethoprim NDC 0121-0853
- Generic Name
- Sulfamethoxazole And Trimethoprim
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSulfatrim NDC 0121-0854
- Generic Name
- Sulfamethoxazole And Trimethoprim
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNystatin NDC 0121-0868
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisolone NDC 0121-0885
- Generic Name
- Prednisolone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenobarbital Oral Solution NDC 0121-0942
- Generic Name
- Phenobarbital Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugDiphenhydramine Hydrochloride NDC 0121-0978
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcetaminophen And Codeine Phosphate NDC 0121-1008
- Generic Name
- Acetaminophen And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 0121-1034
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNystatin NDC 0121-1045
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPromethazine Dm NDC 0121-1070
- Generic Name
- Promethazine Hydrochloride And Dextromethorphan Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0121-1544
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenobarbital Oral Solution NDC 0121-1884
- Generic Name
- Phenobarbital Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0121-2316
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenobarbital Oral Solution NDC 0121-2826
- Generic Name
- Phenobarbital Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0121-4772
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTheophylline NDC 0121-4820
- Generic Name
- Theophylline
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Thirty Spf 30 NDC 0096-0685
- Generic Name
- Solbar Thirty Spf30
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Thirty NDC 0096-0689
- Generic Name
- Sunscreen
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugXerac Ac NDC 0096-0709
- Generic Name
- Xerac Ac
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugAzulfidine En-tabs NDC 0013-0102
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVyndamax NDC 0069-8730
- Generic Name
- Tafamidis
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmaceutical Associates, Inc.
NDC Product
Human Prescription DrugNystatin NDC 0121-0810
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0121-0908
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNystatin NDC 0121-4810
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugProstin Vr Pediatric NDC 0009-0215
- Generic Name
- Alprostadil
- Dosage Form
- Injection, Solution
- Route
- Intravascular; Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProstin Vr Pediatric NDC 0009-3169
- Generic Name
- Alprostadil
- Dosage Form
- Injection, Solution
- Route
- Intravascular; Intravenous
- Marketing
- NDA
Active Listing
Sanofi-Aventis U.S. LLC
NDC Product
Human Prescription DrugJevtana NDC 0024-5824
- Generic Name
- Cabazitaxel
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugAlbuterol Sulfate Hfa NDC 0093-3174
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8739
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8740
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8741
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclosporine Modified NDC 0093-9018
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclosporine Modified NDC 0093-9019
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclosporine Modified NDC 0093-9020
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclosporine NDC 0172-7313
- Generic Name
- Cyclosporine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugElestrin NDC 0037-4801
- Generic Name
- Estradiol
- Dosage Form
- Gel, Metered
- Route
- Topical
- Marketing
- NDA
Active Listing
West-Ward Pharmaceuticals Corp
NDC Product
Human Prescription DrugParicalcitol NDC 0143-9596
- Generic Name
- Paricalcitol
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugParicalcitol NDC 0143-9624
- Generic Name
- Paricalcitol
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugParicalcitol NDC 0143-9625
- Generic Name
- Paricalcitol
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugTorisel NDC 0008-1179
- Generic Name
- Temsirolimus
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Xttrium Laboratories Inc.
NDC Product
Human Prescription DrugValproic Acid NDC 0116-4021
- Generic Name
- Valproic Acid
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc
NDC Product
Human Prescription Drug- Generic Name
- Promethazine Hydrochloride And Dextromethorphan Hydrobromide
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc.
NDC Product
Human Prescription DrugChlorhexidine Gluconate 0.12% Oral Rinse NDC 0116-0003
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Liquid
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorhexidine Gluconate NDC 0116-0101
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNupro Chlorhexidine Gluconate NDC 0116-0800
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorhexidine Gluconate NDC 0116-2001
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0116-4023
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNystatin Oral Suspension NDC 0116-4026
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLidocaine Hydrochloride NDC 0116-4027
- Generic Name
- Lidocaine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral; Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcclean Chlorhexidine Gluconate 0.12% Oral Rinse NDC 0116-4075
- Generic Name
- Chlorhexidine Gluconate 0.12% Oral Rinse
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorhexidine Gluconate NDC 0116-6000
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Rinse
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcclean Chlorhexidine Gluconate 0.12% Oral Rinse NDC 0116-6720
- Generic Name
- Chlorhexidine Gluconate 0.12% Oral Rinse
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- ANDA
Active Listing
