NDC Product
Human Otc DrugTylenol Extra Strength NDC 50090-1695
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Sodium Starch Glycolate Type A, uniquely identified by the FDA Unique Ingredient Identifier (UNII) H8AV0SQX4D.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9063-38-1 and the RxNorm Concept ID (RxCUI) 2360540. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
SODIUM STARCH GLYCOLATE TYPE A
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
H8AV0SQX4D
The specific atomic composition represented as a molecular structure string.
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 Sodium Starch Glycolate Type A. 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
SODIUM CARBOXYMETHYL STARCH
OF
Common Names & Synonyms
CARBOXYMETHYL STARCH SODIUM SALT
CN
SODIUM STARCH GLYCOLATE
CN
SODIUM STARCH GLYCOLATE (TYPE A) [EP MONOGRAPH]
CN
SODIUM STARCH GLYCOLATE [II]
CN
SODIUM STARCH GLYCOLATE [JAN]
CN
SODIUM STARCH GLYCOLATE TYPE A
CN
SODIUM STARCH GLYCOLATE TYPE A [USP-RS]
CN
SODIUM STARCH GLYCOLATE TYPE A, UNSPECIFIED SOURCE
CN
SODIUM STARCH GLYCOLLATE
CN
SODIUM STARCH GLYCOLLATE [WHO-DD]
CN
STARCH, CARBOXYMETHYL ETHER, SODIUM SALT
CN
Brand / Trade Names
COVAGEL
BN
NDC Products Containing SODIUM STARCH GLYCOLATE TYPE A
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
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-6582
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-6626
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-6628
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-7327
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-7329
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-7330
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-7331
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-7332
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7395
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7396
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 50090-7457
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 50090-7458
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 50090-7523
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 50090-7524
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 50090-7582
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 50090-7743
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-7829
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 50090-7882
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugBuspirone Hydrochloride NDC 11788-057
- Generic Name
- Buspirone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuspirone Hydrochloride NDC 11788-058
- Generic Name
- Buspirone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuspirone Hydrochloride NDC 11788-059
- Generic Name
- Buspirone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuspirone Hydrochloride NDC 11788-060
- Generic Name
- Buspirone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuspirone Hydrochloride NDC 11788-061
- Generic Name
- Buspirone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugMetoprolol Tartrate And Hydrochlorothiazide NDC 27241-301
- Generic Name
- Metoprolol Tartrate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Tartrate And Hydrochlorothiazide NDC 27241-302
- Generic Name
- Metoprolol Tartrate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugGood Neighbor Pharmacy Mucus Er NDC 46122-814
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugMesalamine NDC 42291-489
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPazopanib NDC 42291-939
- Generic Name
- Pazopanib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-974
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-975
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-976
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-977
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-978
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-979
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugLoperamide Hydrochloride NDC 50268-482
- Generic Name
- Loperamide Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
BETTER LIVING BRANDS, LLC
NDC Product
Human Otc DrugArthritis Pain NDC 21130-097
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugLoratadine 10mg NDC 21130-932
- Generic Name
- Loratadine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugAleve Back And Muscle Pain NDC 0280-0111
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Headache Pain NDC 0280-0112
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve NDC 0280-0113
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Caplets NDC 0280-0114
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Easy Open Arthritis NDC 0280-0131
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Plus Cold And Flu Fizzychews NDC 0280-0151
- Generic Name
- Chlorpheniramine Maleate, Acetaminophen, Dextromethorphan Hy...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Plus Cough And Sore Throat Fizzychews NDC 0280-0152
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAleve Headache Pain NDC 0280-8252
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Better Living Brands, LLC
NDC Product
Human Otc DrugIbuprofen And Diphenhydramine Citrate NDC 21130-228
- Generic Name
- Ibuprofen And Diphenhydramine Citrate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bi-Mart
NDC Product
Human Otc DrugFamotidine NDC 37835-161
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugFamotidine NDC 37835-165
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugLaxative NDC 37835-241
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 37835-403
- Generic Name
- Guaifenesin, Dextromethorphan Hbr
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMucus Relief NDC 37835-408
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen, Aspirin, And Caffeine NDC 37835-531
- Generic Name
- Acetaminophen, Aspirin, And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMesalamine NDC 31722-043
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-181
- Generic Name
- Topiramate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-182
- Generic Name
- Topiramate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-183
- Generic Name
- Topiramate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-184
- Generic Name
- Topiramate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-284
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-285
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-286
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-287
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-288
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-289
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-290
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-291
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-292
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-293
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-294
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 31722-295
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cintas Corporation
NDC Product
Human Otc DrugFirst Aid Direct Allergy Relief NDC 42961-120
- Generic Name
- Loratadine Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugXpect Pain Away Extra Strength NDC 42961-234
- Generic Name
- Acetaminophen Aspirin Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Contract Pharmacal Corp.
NDC Product
Human Prescription DrugFamotidine NDC 10267-5689
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 10267-5690
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cranbury Pharmaceuticals, LLC
NDC Product
Human Prescription DrugTramadol Hydrochloride NDC 27808-301
- Generic Name
- Tramadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
DORAL PHARMAMEDICS INC dba A.G. Marin Pharmaceuticals
NDC Product
Human Otc DrugNeotuss Plus NDC 12539-779
- Generic Name
- Dextromethorphan Hbr, Chlorpheniramine Maleate, Phenylephrin...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNeotuss Plus NDC 12539-779
- Generic Name
- Dextromethorphan Hbr, Chlorpheniramine Maleate, Phenylephrin...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Dr. Reddy's Laboratories Inc.
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 43598-114
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 43598-115
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 43598-231
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 43598-232
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy's Laboratories Inc.,
NDC Product
Human Prescription DrugEltrombopag NDC 43598-151
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 43598-730
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 43598-731
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 43598-732
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Edenbridge Pharmaceuticals LLC.
NDC Product
Human Prescription DrugVigabatrin NDC 42799-950
- Generic Name
- Vigabatrin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
GenBioPro, Inc.
NDC Product
Human Prescription DrugMisoprostol NDC 43393-024
- Generic Name
- Misoprostol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMisoprostol NDC 43393-200
- Generic Name
- Misoprostol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
HYVEE INC
NDC Product
Human Otc DrugMucus Relief NDC 42507-253
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugExcedrin Extra Strength Headache NDC 0067-2003
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Day NDC 0135-7033
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Night NDC 0135-7034
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
HyVee Inc
NDC Product
Human Otc DrugMucus Er NDC 42507-202
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 42507-414
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMucus Er NDC 42507-471
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugPain Relief NDC 42507-813
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Indoco Remedies Limited
NDC Product
Human Prescription DrugLofexidine NDC 14445-146
- Generic Name
- Lofexidine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc DrugIbuprofen Pm NDC 30142-278
- Generic Name
- Ibuprofen And Diphenhydramine Citrate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugExtra Strength Acetaminophen Pm NDC 30142-755
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMaximum Strength Urinary Pain Relief NDC 30142-756
- Generic Name
- Phenazopyridine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugArthritis Pain Relief NDC 41226-699
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug8 Hour Pain Relief NDC 41226-704
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief NDC 41226-723
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMaximum Strength Mucus Relief NDC 41226-724
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Kroger Company
NDC Product
Human Otc DrugOmeprazole NDC 30142-474
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMucus D NDC 30142-739
- Generic Name
- Guaifenesin And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Sleep Aid Ultra NDC 0113-4032
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Mucus Er NDC 0113-4077
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Dual Action Complete NDC 0113-7050
- Generic Name
- Famotidine, Calcium Carbonate, Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus D NDC 0113-8307
- Generic Name
- Guaifenesin And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus D NDC 0113-8911
- Generic Name
- Guaifenesin, Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company Inc.
NDC Product
Human Prescription DrugMesalamine NDC 0527-3012
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Laurus Labs Limited
NDC Product
Human Prescription DrugFlucytosine NDC 42385-983
- Generic Name
- Flucytosine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlucytosine NDC 42385-984
- Generic Name
- Flucytosine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
MARKSANS PHARMA LIMITED
NDC Product
Human Otc DrugGuaifenesin 1200 Mg NDC 25000-041
- Generic Name
- Guaifenesin 1200 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin 600 Mg NDC 25000-042
- Generic Name
- Guaifenesin 600 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen Extended-release Tablets, 650 Mg NDC 25000-071
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugLoratadine 10mg NDC 25000-092
- Generic Name
- Loratadine 10mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugDexamethasone NDC 0904-7266
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0904-7444
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0904-7451
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0904-7452
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0904-7453
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0904-7552
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0904-7553
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug8hr Arthritis Pain Relief NDC 0904-7561
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorthalidone NDC 0904-7583
- Generic Name
- Chlorthalidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugIsosorbide Dinitrate NDC 0615-8463
- Generic Name
- Isosorbide Dinitrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Dinitrate NDC 0615-8464
- Generic Name
- Isosorbide Dinitrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Dinitrate NDC 0615-8465
- Generic Name
- Isosorbide Dinitrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLoperamide Hydrochloride NDC 0615-8497
- Generic Name
- Loperamide Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0615-8512
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0615-8513
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0615-8518
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugCibinqo NDC 0069-0235
- Generic Name
- Abrocitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVelsipity NDC 0069-0274
- Generic Name
- Etrasimod
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCibinqo NDC 0069-0335
- Generic Name
- Abrocitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCibinqo NDC 0069-0435
- Generic Name
- Abrocitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 16571-113
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 16571-114
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 16571-115
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 16571-126
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 16571-127
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 16571-165
- Generic Name
- Doxazosin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 16571-166
- Generic Name
- Doxazosin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 16571-167
- Generic Name
- Doxazosin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 16571-168
- Generic Name
- Doxazosin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-667
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-668
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-669
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-670
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-671
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-672
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-673
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPhenobarbital NDC 16571-674
- Generic Name
- Phenobarbital
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugLevocarnitine NDC 16571-762
- Generic Name
- Levocarnitine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugMucus Relief Er NDC 0536-1249
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Omeprazole NDC 0536-1448
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugRugby Mucus Relief Er NDC 0536-1451
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
SAFEWAY
NDC Product
Human Otc DrugFamotidine NDC 21130-191
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway
NDC Product
Human Otc DrugAcid Reducer Complete NDC 21130-614
- Generic Name
- Famotidine, Calcium Carbonate And Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcid Reducer Complete NDC 21130-786
- Generic Name
- Famotidine, Calcium Carbonate, Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway, Inc
NDC Product
Human Otc DrugGuaifenesin NDC 21130-554
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
ScieGen Pharmaceuticals Inc
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50228-467
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50228-468
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50228-469
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugMaximum Strength Urinary Pain Relief NDC 11673-270
- Generic Name
- Phenazopyridine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugMotion Sickness Relief NDC 11673-356
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 11673-539
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugArthritis Pain Acetaminophen NDC 11673-673
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 11673-840
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug5-symptom Digestive Relief NDC 11673-880
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug8hr Pain Relief NDC 11673-928
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TIME CAP LABORATORIES, INC.
NDC Product
Human Otc DrugAcetaminophen NDC 49483-699
- Generic Name
- Acetaminophen Tablet Extended Release
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin Extended Release 600 Mg NDC 49483-723
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin Extended Release 1200 Mg NDC 49483-724
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugLoratadine 10 Mg NDC 49483-732
- Generic Name
- Loratadine Tablets Usp, 10 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugSulfasalazine NDC 0093-3234
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugTicagrelor NDC 0480-2688
- Generic Name
- Ticagrelor
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTicagrelor NDC 0480-2695
- Generic Name
- Ticagrelor
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPazopanib NDC 0480-4184
- Generic Name
- Pazopanib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 0480-7750
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugPazopanib NDC 13668-735
- Generic Name
- Pazopanib Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFidaxomicin NDC 13668-745
- Generic Name
- Fidaxomicin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugPain Reliever NDC 0363-6779
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHeadache Relief NDC 0363-7012
- Generic Name
- Acetaminophen, Aspirin, Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugArthritis Pain Reliever NDC 0363-9781
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugMucus Relief D NDC 0363-2389
- Generic Name
- Guaifenesin, Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 0363-3462
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcid Reducer Complete NDC 0363-4036
- Generic Name
- Famotidine, Calcium Carbonate, Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugUltra Sleep Aid NDC 0363-8011
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugGuaifenesin NDC 0363-0570
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0363-9569
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
e5 Pharma, LLC
NDC Product
Human Prescription DrugNitazoxanide NDC 13517-135
- Generic Name
- Nitazoxanide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
