NDC Product
Human Prescription DrugPhenohytro NDC 17856-0125
- Generic Name
- Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Sc...
- Dosage Form
- Elixir
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Fd&c Red No. 3, uniquely identified by the FDA Unique Ingredient Identifier (UNII) PN2ZH5LOQY.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 49746-10-3 and the RxNorm Concept ID (RxCUI) 1366961. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
FD&C RED NO. 3
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
PN2ZH5LOQY
The specific atomic composition represented as a molecular structure string.
InChIKey
C20H6I4O5.2Na.H2O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
IVKWXPBUMQZFCW-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
c1([O-])c(c2c(c(-c3ccccc3C([O-])=O)c4-c(o2)c(c(=O)c(I)c4)I)cc1I)I.[Na+].O.[Na+]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Fd&c Red No. 3. 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
ACID RED 51
OF
AKA3
OF
CI 45430
OF
Common Names & Synonyms
2',4',5',7'-TETRAIODOFLUORESCEIN DISODIUM SALT MONOHYDRATE
CN
9- (O- CARBOXYPHENYL)-6-HYDROXY - 2,4,5,7-TETRAIODO- MONOHYDRATE
CN
C.I. 45430
CN
C.I. ACID RED 51
CN
C.I. FOOD RED 14
CN
DYE FDC RED #3 [VANDF]
CN
E127
CN
ERYTHROSINE
CN
ERYTHROSINE [FCC]
CN
ERYTHROSINE [MART.]
CN
ERYTHROSINE [WHO-DD]
CN
ERYTHROSINE B
CN
ERYTHROSINE SODIUM
CN
ERYTHROSINE SODIUM [USP IMPURITY]
CN
ERYTHROSINE, SODIUM MONOHYDRATE
CN
F D & C RED #3 [VANDF]
CN
F D & C RED #3 ALUMINUM LAKE [VANDF]
CN
F D & C RED NO. 3
CN
FD&C RED 3
CN
FD&C RED NO. 3
CN
FD&C RED NO. 3 [FCC]
CN
FD&C RED NO. 3 [II]
CN
FLUORESCEIN, 2',4',5',7'-TETRAIODO-, DISODIUM SALT
CN
FOOD RED 14
CN
JAPAN RED 3
CN
RED 1799
CN
RED 3
CN
SPIRO(ISOBENZOFURAN-1(3H),9'-(9H)XANTHEN)-3-ONE, 3',6'-DIHYDROXY-2',4',5',7'-TETRAIODO-, DISODIUM SALT, MONOHYDRATE
CN
YELLOW NO. 201
CN
Systematic Nomenclature
DISODIUM 2-(2,4,5,7-TETRAIODO-6-OXIDO-3-OXOXANTHEN-9-YL)BENZOATE
SYS
Technical Codes
C.I.(1975)NO.45430
CD
E-127
CD
INS NO.127
CD
INS-127
CD
NDC Products Containing FD&C RED NO. 3
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
ATLANTIC BIOLOGICALS CORP.
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 17856-2261
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Accord Healthcare, Inc.
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 16729-303
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 16729-304
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 16729-305
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3091
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3092
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3093
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3116
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3117
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3873
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3891
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3895
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3902
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugSilodosin NDC 27241-144
- Generic Name
- Silodosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSilodosin NDC 27241-145
- Generic Name
- Silodosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-227
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-228
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-229
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-230
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allegis Pharmaceuticals, LLC
NDC Product
Human Prescription DrugUrimar-t Caps NDC 28595-224
- Generic Name
- Methenamine, Sodium Phosphate, Monobasic, Monohydrate, Pheny...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugMb Caps NDC 28595-299
- Generic Name
- Methenamine, Sodium Phosphate, Monobasic, Monohydrate, Pheny...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Amneal Pharmaceuticals of New York LLC
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 0115-1325
- 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
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0115-1682
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0115-1685
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0115-9918
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0115-9921
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Arbor Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugErythromycin NDC 24338-120
- Generic Name
- Erythromycin
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAcyclovir NDC 23155-962
- Generic Name
- Acyclovir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 23155-963
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 23155-964
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 23155-965
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 23155-966
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals)
NDC Product
Human Prescription DrugE.e.s NDC 24338-134
- Generic Name
- Erythromycin Ethylsuccinate
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugE.e.s NDC 24338-136
- Generic Name
- Erythromycin Ethylsuccinate
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
BETTER LIVING BRANDS LLC.
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 21130-257
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
BETTER LIVING BRANDS, LLC
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 21130-718
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Better Living Brands LLC
NDC Product
Human Otc DrugAcetaminophen Extra Strength NDC 21130-155
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Better Living Brands, LLC
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 21130-224
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Calvin Scott & Co., Inc.
NDC Product
Human Prescription DrugFluoxetine NDC 17224-171
- Generic Name
- Fluoxetine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluoxetine NDC 17224-174
- Generic Name
- Fluoxetine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 17224-851
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 17224-870
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 31722-052
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 31722-188
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 31722-189
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 31722-195
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-229
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-230
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-231
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-232
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-233
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-234
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-235
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-236
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-350
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Crosstex International Inc.
NDC Product
Human Prescription DrugZap Apf NDC 24794-102
- Generic Name
- Sodium Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugNexium 24hr Clearminis NDC 0573-2452
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Henry Schein Inc.
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0032
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0033
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0034
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0035
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0036
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0037
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0038
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzo-jel NDC 0404-0039
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugCalcitriol NDC 23155-662
- Generic Name
- Calcitriol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCalcitriol NDC 23155-663
- Generic Name
- Calcitriol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
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 DrugMycophenolate Mofetil NDC 0054-0163
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0166
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugColchicine NDC 0143-3018
- Generic Name
- Colchicine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
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 0054-4182
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4184
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4186
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- 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
KROGER COMPANY
NDC Product
Human Otc DrugAcetaminophen Extra Strength NDC 30142-068
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 30142-193
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
KVK-Tech, Inc.
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 10702-026
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 10702-027
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 10702-028
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Kroger Company
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 30142-273
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Esomeprazole Magnesium NDC 0113-0651
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Esomeprazole Magnesium NDC 0113-0898
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Esomeprazole Magnesium NDC 0113-2022
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0527-0586
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4116
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4117
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4118
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4119
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
MARKSANS PHARMA LIMITED
NDC Product
Human Otc DrugEsomeprazole Magnesium Delayed-release Capsules, 20 Mg NDC 25000-075
- Generic Name
- Esomeprazole Magnesium Delayed-release Capsules, 20 Mg
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6269
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6270
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6271
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6272
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugColchicine NDC 0904-6732
- Generic Name
- Colchicine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0904-6987
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0904-6988
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitrofurantoin Macrocrystals NDC 0904-7026
- Generic Name
- Nitrofurantoin Macrocrystals
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClomipramine Hydrochloride NDC 0904-7038
- Generic Name
- Clomipramine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClomipramine Hydrochloride NDC 0904-7039
- Generic Name
- Clomipramine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCalcium Acetate NDC 0904-7119
- Generic Name
- Calcium Acetate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenytoin Sodium NDC 0904-7416
- Generic Name
- Phenytoin Sodium
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitrofurantoin (monohydrate/macrocrystals) NDC 0904-7571
- Generic Name
- Nitrofurantoin (monohydrate/macrocrystals)
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugTacrolimus NDC 0378-2046
- Generic Name
- Tacrolimus
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTacrolimus NDC 0378-2047
- Generic Name
- Tacrolimus
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclofenamate Sodium NDC 0378-2150
- Generic Name
- Meclofenamate Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclofenamate Sodium NDC 0378-3000
- Generic Name
- Meclofenamate Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0378-8030
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 0615-8344
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0615-8442
- Generic Name
- Potassium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar Rx LLC
NDC Product
Human Prescription DrugCefprozil NDC 16714-396
- Generic Name
- Cefprozil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefprozil NDC 16714-397
- Generic Name
- Cefprozil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 16714-835
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 16714-836
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 16714-837
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 16714-838
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar RxLLC
NDC Product
Human Prescription DrugItraconazole NDC 16714-743
- Generic Name
- Itraconazole
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 16714-553
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 16714-554
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 16714-555
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 16714-759
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 16714-760
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 16714-761
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 16714-824
- Generic Name
- Potassium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
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
Par Health USA, LLC
NDC Product
Human Prescription DrugAlvimopan NDC 0254-3012
- Generic Name
- Alvimopan
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugZarontin NDC 0071-0237
- Generic Name
- Ethosuximide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugNorpace Cr NDC 0025-2732
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace Cr NDC 0025-2742
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace NDC 0025-2752
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace NDC 0025-2762
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugMedrol NDC 0009-0020
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0022
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0056
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0073
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 16571-260
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropafenone Hydrochloride NDC 16571-736
- Generic Name
- Propafenone Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropafenone Hydrochloride NDC 16571-737
- Generic Name
- Propafenone Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropafenone Hydrochloride NDC 16571-738
- Generic Name
- Propafenone Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 11822-0024
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugPain Relief Acetaminophen Pm NDC 11822-0556
- Generic Name
- Acetaminophen And Diphenhydramine Hcl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 11822-0898
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
SUNRISE PHARMACEUTICAL, INC.
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 11534-157
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 11534-159
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 11534-176
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway
NDC Product
Human Otc DrugSignature Care Esomeprazole Magnesium NDC 21130-088
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Esomeprazole Magnesium NDC 21130-714
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway, Inc.
NDC Product
Human Otc DrugEsomeprazole NDC 21130-926
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2299
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2479
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2480
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2481
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0804
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0807
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5111
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5112
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5113
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5114
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5115
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5116
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5117
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9914
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9915
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9916
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9917
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemazepam NDC 0406-9959
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemazepam NDC 0406-9960
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Supernus Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-102
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-103
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-104
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
THE KROGER COMPANY
NDC Product
Human Otc DrugEsomeprazole NDC 30142-989
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Target Corporation
NDC Product
Human Otc DrugUp And Up Esomeprazole Magnesium NDC 11673-753
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugUp And Up Esomeprazole Magnesium NDC 11673-898
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 24979-138
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 24979-139
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 24979-181
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 24979-182
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 24979-183
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugEsomeprazole Magnesium Delayed Release NDC 0363-7810
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugPain Reliever Pm Extra Strength NDC 0363-0556
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMulti-symptom Allergy NDC 0363-0559
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-1699
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-7223
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
