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 Fd&c Yellow No. 6, uniquely identified by the FDA Unique Ingredient Identifier (UNII) H77VEI93A8.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 2783-94-0 and the RxNorm Concept ID (RxCUI) 1305574. 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 YELLOW NO. 6
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
H77VEI93A8
The specific atomic composition represented as a molecular structure string.
InChIKey
C16H10N2O7S2.2Na International Chemical Identifier digital signature for unique molecular identification.
SMILES String
OIQPTROHQCGFEF-QIKYXUGXSA-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
c1c2c(ccc(c2)S([O-])(=O)=O)c(c(c1)O)/N=N/c3ccc(cc3)S([O-])(=O)=O.[Na+].[Na+]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Fd&c Yellow No. 6. 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
CI 15985
OF
KI5
OF
SUNSET YELLOW
OF
YELLOW 6
OF
Common Names & Synonyms
2-NAPHTHALENESULFONIC ACID, 6-HYDROXY-5-((E)-(4-SULFOPHENYL)AZO)-, DISODIUM SALT
CN
C.I. FOOD YELLOW 3
CN
C.I. FOOD YELLOW 3 [HSDB]
CN
CI-FOOD YELLOW 3
CN
COLOUR INDEX NO. 15985
CN
CRELBORANGE S
CN
D&C YELLOW NO. 6
CN
D&C YELLOW NO. 6 [II]
CN
DISODIUM SALT OF 6-HYDROXY-5-((4-SULFOPHENYL)AZO)-2-NAPHTHALENESULFONIC ACID
CN
DYE DC YELLOW NO. 6
CN
DYE FDC YELLOW NO. 6
CN
DYE YELLOW NO. 6
CN
F D & C YELLOW #6
CN
F D & C YELLOW NO. 6
CN
FD&C YELLOW 6
CN
FD&C YELLOW NO. 6
CN
FD&C YELLOW NO. 6 [FCC]
CN
FD&C YELLOW NO. 6 [II]
CN
FD&C YELLOW NO.6
CN
FDC YELLOW NO. 6
CN
ORANGE YELLOW S
CN
SUNSET YELLOW [FCC]
CN
SUNSET YELLOW FCF
CN
SUNSET YELLOW FCF [IARC]
CN
SUNSET YELLOW FCF [MART.]
CN
SUNSET YELLOW FCF [MI]
CN
Systematic Nomenclature
DISODIUM 6-HYDROXY-5-((E)-(4-SULFONATOPHENYL)DIAZENYL)NAPHTHALENE-2-SULFONATE
SYS
Technical Codes
CI (1975) NO. 15985
CD
CI-(1975)-NO.15985
CD
CI-15985
CD
E110
CD
E-110
CD
INS NO.110
CD
INS-110
CD
NDC Products Containing FD&C YELLOW NO. 6
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 DrugNorvir NDC 0074-3399
- Generic Name
- Ritonavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-3727
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-4341
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-4552
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-5182
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-6594
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-6624
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7068
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7069
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7070
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7148
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7149
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-9296
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1231
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1232
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1233
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1234
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1315
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1316
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1317
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, 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 DrugCyclobenzaprine Hydrochloride NDC 0115-1437
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMetaxalone NDC 0115-1745
- Generic Name
- Metaxalone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1800
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1801
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1802
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRimantadine Hydrochloride NDC 0115-1911
- Generic Name
- Rimantadine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDantrolene Sodium NDC 0115-4433
- Generic Name
- Dantrolene Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 0115-5445
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 0115-5511
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 0115-5522
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0115-9927
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0115-9928
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0115-9929
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Soft Chews NDC 0067-0111
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Tablet, Chewable
- 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 DrugGas-x Ultra Strength Antigas Softgels NDC 0067-6274
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6801
- Generic Name
- Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine ...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Tension Headache NDC 0067-8139
- Generic Name
- Acetaminophen, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength And Excedrin Tension Headache NDC 0067-8151
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr And Acetaminophen, Chlor...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0273
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0274
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0275
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0276
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride NDC 0054-0750
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugCalcitriol NDC 0054-0007
- Generic Name
- Calcitriol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBalsalazide Disodium NDC 0054-0079
- Generic Name
- Balsalazide Disodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
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 DrugRamipril NDC 0054-0106
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0107
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0108
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0109
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihyd...
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihyd...
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0371
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0372
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0373
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0374
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0375
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0400
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0401
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0603
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- 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 DrugFurosemide NDC 0054-3294
- Generic Name
- Furosemide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-3298
- Generic Name
- Furosemide
- 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 DrugNaproxen NDC 0054-3630
- Generic Name
- Naproxen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiskets NDC 0054-4538
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- 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 0054-4179
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- 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
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 Pain Relief NDC 0113-0025
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
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 Aspirin NDC 0113-0467
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Stool Softener NDC 0113-0486
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Daytime Cold And Flu NDC 0113-0603
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Daytime Non Drowsy Cold And Flu NDC 0113-0656
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Gas Relief NDC 0113-0657
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Aller Ease NDC 0113-0847
- Generic Name
- Fexofenadine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Daytime NDC 0113-0994
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Lice Killing Creme Rinse NDC 0113-1910
- Generic Name
- Permethrin
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Day Time Cold And Flu NDC 0113-2299
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Ibuprofen NDC 0113-2461
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time Cold And Flu NDC 0113-2501
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Day Time Cold And Flu NDC 0113-4500
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugTegretol NDC 0078-0508
- Generic Name
- Carbamazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol NDC 0078-0509
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0510
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0511
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0512
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTykerb NDC 0078-0671
- Generic Name
- Lapatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
PAI Holdings, LLC
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-0775
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Prescription DrugMetoclopramide NDC 0121-0576
- Generic Name
- Metoclopramide Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEthosuximide NDC 0121-0670
- Generic Name
- Ethosuximide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTricitrates NDC 0121-0677
- Generic Name
- Potassium Citrate, Sodium Citrate, And Citric Acid Monohydra...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugTheophylline NDC 0121-0820
- Generic Name
- Theophylline
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugDilantin Infatabs NDC 0071-0007
- Generic Name
- Phenytoin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelontin NDC 0071-0525
- Generic Name
- Methsuximide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZarontin NDC 0071-2418
- Generic Name
- Ethosuximide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
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
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0093-0318
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0093-0319
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0093-0320
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0093-0321
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLovastatin NDC 0093-0576
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0810
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0811
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0812
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0813
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLovastatin NDC 0093-0926
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLovastatin NDC 0093-0928
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiclofenac Potassium NDC 0093-0948
- Generic Name
- Diclofenac Potassium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefprozil NDC 0093-1077
- Generic Name
- Cefprozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefprozil NDC 0093-1078
- Generic Name
- Cefprozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 DrugAcitretin NDC 0093-1136
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1715
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1716
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1718
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1720
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1721
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-1921
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-2063
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisedronate Sodium NDC 0093-3098
- Generic Name
- Risedronate Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCamrese NDC 0093-3134
- Generic Name
- Levonorgestrel / Ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5002
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5003
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5348
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5503
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5504
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5505
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5506
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5507
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRivelsa NDC 0093-6031
- Generic Name
- Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugCamrese Lo NDC 0093-6148
- Generic Name
- Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA AUTHORIZED GENERIC
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 DrugVenlafaxine Hydrochloride NDC 0093-7384
- Generic Name
- Venlafaxine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVenlafaxine Hydrochloride NDC 0093-7385
- Generic Name
- Venlafaxine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVenlafaxine Hydrochloride NDC 0093-7386
- Generic Name
- Venlafaxine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImatinib Mesylate NDC 0093-7629
- Generic Name
- Imatinib Mesylate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImatinib Mesylate NDC 0093-7630
- Generic Name
- Imatinib Mesylate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8162
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8163
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8164
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8165
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8166
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0093-8192
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0093-8204
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8224
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8229
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8231
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0093-8305
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugEletriptan Hydrobromide NDC 0093-8310
- Generic Name
- Eletriptan Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEletriptan Hydrobromide NDC 0093-8311
- Generic Name
- Eletriptan Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlyburide NDC 0093-8343
- Generic Name
- Glyburide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlyburide NDC 0093-8344
- Generic Name
- Glyburide
- Dosage Form
- Tablet
- 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
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 DrugCarbidopa And Levodopa NDC 0093-9702
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugPristiq Extended-release NDC 0008-1210
- Generic Name
- Desvenlafaxine Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPristiq Extended-release NDC 0008-1222
- Generic Name
- Desvenlafaxine Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1100
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1103
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1104
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
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 DrugLactulose NDC 0116-4005
- Generic Name
- Lactulose
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
