NDC Product
Human Prescription DrugSynthroid NDC 0074-3727
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for D&c Yellow No. 10, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 35SW5USQ3G.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 8004-92-0 and the RxNorm Concept ID (RxCUI) 1305564. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
D&C YELLOW NO. 10
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
35SW5USQ3G
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
mixture
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for D&c Yellow No. 10. 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 YELLOW 3
OF
CI 47005
OF
KI203
OF
YELLOW 10
OF
Common Names & Synonyms
BASOVIT YELLOW-095E
CN
C YELLOW NO. 10
CN
C.I. ACID YELLOW 3
CN
C.I. ACID YELLOW 3 DISODIUM SALT
CN
CI (1975) NO. 47005
CN
CI FOOD YELLOW 13
CN
CI-FOOD YELLOW-13
CN
COGILOR YELLOW-112.12
CN
D & C YELLOW #10 [VANDF]
CN
D & C YELLOW NO. 10
CN
D&C YELLOW NO. 10
CN
D&C YELLOW NO. 10 [II]
CN
DC YELLOW NO. 10
CN
E-104
CN
EUROCERT QUINOLINE YELLOW-311744
CN
F D & C YELLOW #10 [VANDF]
CN
FD&C YELLOW NO. 10 (DELISTED)
CN
FD&C YELLOW NO. 10 (DELISTED) [II]
CN
FOOD YELLOW 13
CN
INS NO.104
CN
NEELICOL QUINOLINE YELLOW-WS
CN
QUINOLINE YELLOW
CN
QUINOLINE YELLOW [MART.]
CN
QUINOLINE YELLOW [MI]
CN
QUINOLINE YELLOW [USP-RS]
CN
QUINOLINE YELLOW OXIDE (E104)
CN
QUINOLINE YELLOW WS
CN
QUINOLINE YELLOW-104
CN
SODIUM 2-(1,3-DIOXOINDAN-2-YL)QUINOLINEDISULFONATE
CN
VITASYN QUINOLINE YELLOW-70
CN
Technical Codes
CI-(1975)-NO.47005
CD
E104
CD
INS-104
CD
NDC Products Containing D&C YELLOW NO. 10
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 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
Haleon US Holdings LLC
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8655
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8725
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8726
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, And Doxylamine...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8753
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8754
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8755
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-0100
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Honey Ginger NDC 0067-0103
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0122
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0123
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Extra Strength NDC 0067-0129
- Generic Name
- Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Geltabs NDC 0067-2021
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Geltabs NDC 0067-2035
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugTheraflu Powerpods Nighttime Severe Cold NDC 0067-6095
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Extra Strength Softgels NDC 0067-6275
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Multi-symptom Severe Cold NDC 0067-6426
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-6802
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6803
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Nighttime Severe Cold And Cough NDC 0067-7918
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-7921
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-7922
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, And Acetaminophen, Chlo...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc
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 DrugFebuxostat NDC 0054-0413
- Generic Name
- Febuxostat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 0054-0414
- Generic Name
- Febuxostat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProgesterone NDC 0054-0829
- Generic Name
- Progesterone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProgesterone NDC 0054-0830
- Generic Name
- Progesterone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugZaleplon NDC 0054-0084
- Generic Name
- Zaleplon
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0085
- Generic Name
- Zaleplon
- 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 DrugGalantamine Hydrobromide NDC 0054-0137
- Generic Name
- Galantamine Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam Intensol NDC 0054-3185
- Generic Name
- Diazepam Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam NDC 0054-3188
- Generic Name
- Diazepam
- 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 DrugLeucovorin Calcium NDC 0054-4498
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-4499
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-8496
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugDexamethasone Intensol NDC 0054-3176
- Generic Name
- Dexamethasone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-3177
- Generic Name
- Dexamethasone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4179
- 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 Nicotine NDC 0113-0053
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-0056
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0170
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Anti Diarrheal NDC 0113-0224
- Generic Name
- Loperamide Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-0335
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Cough Dm NDC 0113-0384
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0422
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Gas Relief Extra Strength NDC 0113-0428
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0532
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- 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 DrugZarontin NDC 0071-0237
- Generic Name
- Ethosuximide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCelontin NDC 0071-0525
- Generic Name
- Methsuximide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugFlagyl NDC 0025-1942
- Generic Name
- Metronidazole
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugPiroxicam NDC 0093-0756
- Generic Name
- Piroxicam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPiroxicam NDC 0093-0757
- Generic Name
- Piroxicam
- Dosage Form
- Capsule
- 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 0093-0928
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- 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
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1135
- 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 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 DrugAcitretin NDC 0093-1138
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1714
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
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 0093-1920
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
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 DrugAmoxicillin NDC 0093-2267
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2268
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- 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 DrugRisedronate Sodium NDC 0093-3099
- Generic Name
- Risedronate Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisedronate Sodium NDC 0093-3100
- Generic Name
- Risedronate Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-3107
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-3109
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicloxacillin Sodium NDC 0093-3123
- Generic Name
- Dicloxacillin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicloxacillin Sodium NDC 0093-3125
- Generic Name
- Dicloxacillin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDisopyramide Phosphate NDC 0093-3127
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDisopyramide Phosphate NDC 0093-3129
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule
- 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 DrugCephalexin NDC 0093-3145
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-3147
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-3160
- Generic Name
- Cefdinir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefadroxil NDC 0093-3196
- Generic Name
- Cefadroxil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClonazepam NDC 0093-3212
- Generic Name
- Clonazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClonazepam NDC 0093-3213
- Generic Name
- Clonazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3543
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3544
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3545
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3546
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3547
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3548
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4067
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4068
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4069
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-4155
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4175
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4177
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
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 DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5004
- 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 0093-5006
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5045
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5046
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugJunel Fe 24 NDC 0093-5328
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5346
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5347
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- 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 DrugAtazanavir Sulfate NDC 0093-5526
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5527
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5528
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5550
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5551
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5552
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5553
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5554
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5562
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- 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
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7163
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7164
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- 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 DrugFluoxetine NDC 0093-7198
- Generic Name
- Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0093-7334
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLosartan Potassium And Hydrochlorothiazide NDC 0093-7367
- Generic Name
- Losartan Potassium And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLosartan Potassium And Hydrochlorothiazide NDC 0093-7368
- Generic Name
- Losartan Potassium And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLosartan Potassium And Hydrochlorothiazide NDC 0093-7369
- Generic Name
- Losartan Potassium And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- 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 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
Human Prescription DrugCimetidine NDC 0093-8204
- 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 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 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
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 0093-8740
- 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
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8741
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
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
