NDC Product
Human Prescription DrugVenclexta NDC 0074-0561
- Generic Name
- Venetoclax
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Anhydrous Dibasic Calcium Phosphate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) L11K75P92J.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7757-93-9 and the RxNorm Concept ID (RxCUI) 47627. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
L11K75P92J
The specific atomic composition represented as a molecular structure string.
InChIKey
Ca.HO4P International Chemical Identifier digital signature for unique molecular identification.
SMILES String
FUFJGUQYACFECW-UHFFFAOYSA-L 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
P([O-])([O-])(=O)O.[Ca+2]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Anhydrous Dibasic Calcium Phosphate. 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
DICALCIUM PHOSPHATE
OF
Common Names & Synonyms
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
CN
ANHYDROUS DIBASIC CALCIUM PHOSPHATE [JAN]
CN
ANHYDROUS DIBASIC CALCIUM PHOSPHATE [USP MONOGRAPH]
CN
CALCII HYDROGENOPHOSPHAS [WHO-IP LATIN]
CN
CALCIUM (AS PHOSPHATE,DIBASIC) [VANDF]
CN
CALCIUM (CALCIUM PHOSPHATE (DIBASIC))
CN
CALCIUM HYDROGEN PHOSPHATE (ANHYDROUS)
CN
CALCIUM HYDROGEN PHOSPHATE [EP MONOGRAPH]
CN
CALCIUM HYDROGEN PHOSPHATE ANHYDROUS
CN
CALCIUM HYDROGEN PHOSPHATE, ANHYDROUS [WHO-IP]
CN
CALCIUM PHOSPHATE (1:1) [WHO-IP]
CN
CALCIUM PHOSPHATE (DIBASIC)
CN
CALCIUM PHOSPHATE DIBASIC
CN
CALCIUM PHOSPHATE DIBASIC [WHO-DD]
CN
CALCIUM PHOSPHATE, DIBASIC
CN
CALCIUM PHOSPHATE, DIBASIC [HSDB]
CN
CALCIUM PHOSPHATE, DIBASIC [MI]
CN
CALCIUM PHOSPHATE, DIBASIC ANHYDROUS
CN
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
CN
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS [II]
CN
CALCIUM PHOSPHATE,DIBASIC [VANDF]
CN
DIBASIC CALCIUM PHOSPHATE
CN
DIBASIC CALCIUM PHOSPHATE ANHYDROUS
CN
PHOSPHORIC ACID, CALCIUM SALT (1:1)
CN
PHOSPHORUS (AS CALCIUM PHOSPHATE,DIBASIC) [VANDF]
CN
PHOSPHORUS (AS DICALCIUM PHOSPHATE)
CN
PHOSPHORUS (AS DICALCIUM PHOSPHATE) [VANDF]
CN
SECONDARY CALCIUM PHOSPHATE
CN
Brand / Trade Names
A-COMPREZ
BN
Systematic Nomenclature
CALCIUM HYDROGEN MONOPHOSPHATE
SYS
CALCIUM HYDROGEN ORTHOPHOSPHATE
SYS
CALCIUM HYDROGEN PHOSPHATE
SYS
CALCIUM MONOHYDROGEN PHOSPHATE
SYS
CALCIUM PHOSPHATE (1:1)
SYS
DICALCIUM ORTHOPHOSPHATE
SYS
Technical Codes
E-341(II)
CD
INS NO.341(II)
CD
INS-341(II)
CD
NDC Products Containing ANHYDROUS DIBASIC CALCIUM PHOSPHATE
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 DrugVenclexta NDC 0074-0566
- Generic Name
- Venetoclax
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVenclexta NDC 0074-0576
- Generic Name
- Venetoclax
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVenclexta NDC 0074-0579
- Generic Name
- Venetoclax
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorvir NDC 0074-3399
- Generic Name
- Ritonavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
Acme United Corporation
NDC Product
Human Otc DrugPhysicianscare Allergy Antihistamine NDC 0924-0056
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugDoxepin NDC 0228-3315
- Generic Name
- Doxepin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Doxepin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Doxepin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDoxepin NDC 0228-3316
- Generic Name
- Doxepin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPentazocine And Naloxone NDC 0591-0395
- Generic Name
- Pentazocine Hydrochloride And Naloxone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Pentazocine Hydrochloride And Naloxone Hydrochloride
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDalfampridine NDC 0591-2533
- Generic Name
- Dalfampridine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Trihexyphenidyl Hydrochloride
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTrihexyphenidyl Hydrochloride NDC 0591-5335
- Generic Name
- Trihexyphenidyl Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTrihexyphenidyl Hydrochloride NDC 0591-5337
- Generic Name
- Trihexyphenidyl Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Trihexyphenidyl Hydrochloride
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAmoxapine NDC 0591-5713
- Generic Name
- Amoxapine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxapine NDC 0591-5714
- Generic Name
- Amoxapine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxapine NDC 0591-5715
- Generic Name
- Amoxapine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxapine NDC 0591-5716
- Generic Name
- Amoxapine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Labs LLC
NDC Product
Human Prescription DrugGlycopyrrolate NDC 15955-305
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlycopyrrolate NDC 15955-318
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurolife Pharma LLC
NDC Product
Human Prescription DrugParoxetine NDC 13107-154
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-155
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-156
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-157
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Basic Drugs, Inc.
NDC Product
Human Otc DrugNatural Senna Laxative NDC 0761-0790
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSenna Laxative NDC 0761-0798
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSenna-s Laxative With Stool Softener NDC 0761-0910
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bausch Health US LLC
NDC Product
Human Prescription DrugTasmar NDC 0187-0938
- Generic Name
- Tolcapone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugClaritin-d 12 Hour NDC 11523-7162
- Generic Name
- Loratadine And Pseudoephedrine Sulfate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc Drug- Generic Name
- Zinc Acetate Anhydrous And Zinc Gluconate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugZicam Cold Remedy Medicated Fruit Drops - Assorted Fruit NDC 10237-468
- Generic Name
- Zinc Acetate Anhydrous And Zinc Gluconate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugZicam Cold Remedy Medicated Fruit Drops - Elderberry NDC 10237-469
- Generic Name
- Zinc Acetate Anhydrous, Zinc Gluconate, And Sambucus Nigra F...
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
DORAL PHARMAMEDICS INC dba A.G. Marin Pharmaceuticals
NDC Product
Human Prescription DrugUretron D/s NDC 12539-144
- Generic Name
- Methenamine, Sodium Phosphate Monobasic, Phenyl Salicylate, ...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Exeltis USA, Inc
NDC Product
Human Prescription DrugVitafol-ob Plus Dha Prenatal Supplement Plus Dha NDC 0642-0076
- Generic Name
- Vitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Exeltis USA, Inc.
NDC Product
Human Prescription DrugVitafol One NDC 0642-0070
- Generic Name
- Prenatal Supplement With Dha
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSelect-ob Plus Dha Prenatal Supplement Plus Dha NDC 0642-0075
- Generic Name
- .beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalc...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugStrovite One Caplets NDC 0642-0207
- Generic Name
- Vitamin A, Calcium Pantothenate, Ascorbic Acid, Cholecalcife...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
GlaxoSmithKline LLC
NDC Product
Human Prescription DrugImitrex NDC 0173-0735
- Generic Name
- Sumatriptan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugImitrex NDC 0173-0736
- Generic Name
- Sumatriptan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugImitrex NDC 0173-0737
- Generic Name
- Sumatriptan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugEx-lax Regular Strength Stimulant Laxative NDC 0067-8141
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEx-lax Maximum Strength Stimulant Laxative NDC 0067-8142
- Generic Name
- Sennosides
- Dosage Form
- Pill
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPerdiem NDC 0067-8143
- Generic Name
- Sennosides, Stimulant Laxative
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCitrucel NDC 0135-0089
- Generic Name
- Methylcellulose
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCitrucel NDC 0135-0090
- Generic Name
- Methylcellulose
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCitrucel NDC 0135-0199
- Generic Name
- Methylcellulose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8050
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8060
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cherry Peppermint NDC 0135-8070
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cherry Peppermint NDC 0135-8071
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugSapropterin Dihydrochloride NDC 0054-0906
- Generic Name
- Sapropterin Dihydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Anti Diarrheal Anti Gas NDC 0113-0087
- Generic Name
- Loperamide Hydrochloride, Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Aid NDC 0113-0441
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Anti Diarrheal Anti Gas NDC 0113-1087
- Generic Name
- Loperamide Hydrochloride, Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAllergy And Congestion Relief NDC 0113-2007
- Generic Name
- Loratadine, Pseudoephedrine Sulfate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Aid Ultra NDC 0113-4032
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Aid Ultra NDC 0113-6044
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugPerrigo Allergy D NDC 0113-7777
- Generic Name
- Loratadine, Pseudoephedrine Sulfate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Laser Pharmaceuticals, LLC
NDC Product
Human Prescription DrugHyoscyamine Sulfate NDC 16477-738
- Generic Name
- Hyoscyamine Sulfate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
MAJOR PHARMACEUTICALS
NDC Product
Human Otc DrugDok NDC 0904-6750
- Generic Name
- Docusate Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Major Pharmaceuticals
NDC Product
Human Otc DrugDriminate NDC 0904-2051
- Generic Name
- Dimenhydrinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBanophen NDC 0904-5551
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugFluconazole NDC 0904-6500
- Generic Name
- Fluconazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluconazole NDC 0904-6501
- Generic Name
- Fluconazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 0904-6671
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0904-6797
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0904-6798
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0904-6799
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhytonadione NDC 0904-6882
- Generic Name
- Phytonadione
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0904-6924
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0904-6925
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0904-6926
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugPseudoephedrine Hcl NDC 0904-6990
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0904-7350
- Generic Name
- Azithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0904-7351
- Generic Name
- Azithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClonidine Hydrochloride NDC 0904-7442
- Generic Name
- Clonidine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 10135-740
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 10135-741
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 10135-742
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 10135-808
- Generic Name
- Varenicline Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 10135-809
- Generic Name
- Varenicline Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugJanuvia NDC 0006-0112
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanuvia NDC 0006-0221
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0227
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanuvia NDC 0006-0277
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0473
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0477
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3080
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3603
- Generic Name
- Raltegravir
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglujan NDC 0006-5367
- Generic Name
- Ertugliflozin And Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglujan NDC 0006-5368
- Generic Name
- Ertugliflozin And Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugMetoclopramide NDC 0615-7698
- Generic Name
- Metoclopramide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0615-8252
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0615-8253
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0615-8254
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0615-8255
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0615-8359
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0615-8405
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine Besylate NDC 0615-8430
- Generic Name
- Amlodipine Besylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 0615-8532
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 0615-8533
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 0615-8534
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 0615-8535
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0615-8596
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0615-8603
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0615-8604
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
PFIZER LABORATORIES DIV PFIZER INC
NDC Product
Human Prescription DrugRevatio NDC 0069-4190
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Padagis US LLC
NDC Product
Human Prescription DrugParoxetine NDC 0574-0279
- Generic Name
- Paroxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmiloride Hydrochloride NDC 0574-0292
- Generic Name
- Amiloride Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugLorbrena NDC 0069-0227
- Generic Name
- Lorlatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLorbrena NDC 0069-0231
- Generic Name
- Lorlatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCibinqo NDC 0069-0235
- Generic Name
- Abrocitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDaurismo NDC 0069-0298
- Generic Name
- Glasdegib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCibinqo NDC 0069-0335
- Generic Name
- Abrocitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCibinqo NDC 0069-0435
- Generic Name
- Abrocitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugChantix NDC 0069-0468
- Generic Name
- Varenicline Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugChantix NDC 0069-0469
- Generic Name
- Varenicline Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugChantix NDC 0069-0471
- Generic Name
- Varenicline Tartrate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDaurismo NDC 0069-1531
- Generic Name
- Glasdegib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3060
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3070
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3120
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3130
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3140
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-4061
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxlovid NDC 0069-5045
- Generic Name
- Nirmatrelvir And Ritonavir
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxlovid NDC 0069-5317
- Generic Name
- Nirmatrelvir And Ritonavir
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxlovid NDC 0069-5321
- Generic Name
- Nirmatrelvir And Ritonavir
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXalkori NDC 0069-8140
- Generic Name
- Crizotinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXalkori NDC 0069-8141
- Generic Name
- Crizotinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharbest Pharmaceuticals, Inc.
NDC Product
Human Otc DrugSenna Tabs NDC 16103-363
- Generic Name
- Senna
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMeclizine NDC 16103-386
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
RUGBY LABORATORIES
NDC Product
Human Otc DrugMeclizine NDC 0536-1297
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-660
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-661
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-662
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-663
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugGlycopyrrolate NDC 16571-743
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugSinus Pressure And Congestion Relief Maximum Strength NDC 11822-0112
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMotion Sickness Relief NDC 11822-0198
- Generic Name
- Dimenhydrinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 11822-0441
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAllergy Relief D NDC 11822-1055
- Generic Name
- Loratadine, Pseudoephedrine Sulfate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 11822-3000
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Roerig
NDC Product
Human Prescription DrugDiflucan NDC 0049-3450
- Generic Name
- Fluconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugGriseofulvin NDC 0781-5514
- Generic Name
- Griseofulvin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGriseofulvin NDC 0781-5515
- Generic Name
- Griseofulvin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin Phosphate NDC 0781-5766
- Generic Name
- Sitagliptin Phosphate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin Phosphate NDC 0781-5768
- Generic Name
- Sitagliptin Phosphate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin Phosphate NDC 0781-5770
- Generic Name
- Sitagliptin Phosphate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
TEVA Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugGlyburide NDC 0093-9364
- Generic Name
- Glyburide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugGlyburide NDC 0093-9433
- Generic Name
- Glyburide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugGlyburide NDC 0093-9477
- Generic Name
- Glyburide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Target Corporation
NDC Product
Human Otc DrugUp And Up Nighttime Sleep Aid NDC 11673-171
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugUp And Up Anti Diarrheal Anti Gas NDC 11673-646
- Generic Name
- Loperamide Hydrochloride, Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugEtodolac NDC 0093-1118
- Generic Name
- Etodolac
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtodolac NDC 0093-1122
- Generic Name
- Etodolac
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-1172
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-1174
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoclopramide NDC 0093-2203
- Generic Name
- Metoclopramide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoclopramide NDC 0093-2204
- Generic Name
- Metoclopramide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 0093-3241
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 0093-3242
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 0093-3243
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-3420
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-3421
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-3422
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-4125
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-4127
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 0093-5341
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 0093-5342
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 0093-5343
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtodolac NDC 0093-7172
- Generic Name
- Etodolac
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 0172-2083
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 0172-2089
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugAmlodipine Besylate NDC 0480-0083
- Generic Name
- Amlodipine Besylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTicagrelor NDC 0480-2688
- Generic Name
- Ticagrelor
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTicagrelor NDC 0480-2695
- Generic Name
- Ticagrelor
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine Besylate NDC 0480-7167
- Generic Name
- Amlodipine Besylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine Besylate NDC 0480-7168
- Generic Name
- Amlodipine Besylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPravastatin Sodium NDC 0480-7270
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugSildenafil NDC 13668-185
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 13668-186
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 13668-187
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 13668-188
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugUrelle NDC 0037-6321
- Generic Name
- Hyoscyamine Sulfate, Methenamine, Methylene Blue, Phenyl Sal...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugLoperamide Hydrochloride And Simethicone NDC 0363-9606
- Generic Name
- Loperamide Hydrochloride And Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugAnti Diarrheal And Anti Gas NDC 0363-1830
- Generic Name
- Loperamide Hydrochloride, Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAwake Maximum Strength NDC 0363-3440
- Generic Name
- Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 0363-3462
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAllergy Relief D 12 NDC 0363-7023
- Generic Name
- Loratadine, Pseudoephedrine Sulfate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugUltra Sleep Aid NDC 0363-8011
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens Company
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 0363-0042
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
