NDC Product
Human Prescription DrugSymbicort NDC 50090-1403
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Povidone K25, uniquely identified by the FDA Unique Ingredient Identifier (UNII) K0KQV10C35.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9003-39-8 and the RxNorm Concept ID (RxCUI) 1367141. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
POVIDONE K25
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
K0KQV10C35
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Povidone K25. 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.
Common Names & Synonyms
POVIDONE K22.5-27
CN
POVIDONE K25
CN
POVIDONE K25 [II]
CN
Brand / Trade Names
KOLLIDON 25
BN
PLASDONE K-25
BN
NDC Products Containing POVIDONE K25
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 (383), 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 DrugEtodolac NDC 50090-2132
- Generic Name
- Etodolac
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDrospirenone And Ethinyl Estradiol NDC 50090-2494
- Generic Name
- Drospirenone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDrospirenone And Ethinyl Estradiol NDC 50090-2594
- Generic Name
- Drospirenone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-3747
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSymbicort NDC 50090-4508
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSymbicort NDC 50090-4509
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSymbicort NDC 50090-4510
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 50090-6322
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide And Formoterol Fumarate Dihydrate NDC 50090-6327
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugBudesonide And Formoterol Fumarate Dihydrate NDC 50090-6382
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 50090-6394
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 50090-6426
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-6908
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-6909
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-7082
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-7083
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 50090-7628
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 50090-7656
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 50090-7657
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 50090-7823
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Accord Healthcare, Inc.
NDC Product
Human Prescription DrugSpironolactone NDC 16729-225
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 16729-226
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 16729-227
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ahold U.S.A., Inc,
NDC Product
Human Otc DrugMucus Relief Dm NDC 60000-057
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 60000-058
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugFenofibrate NDC 27241-118
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 27241-119
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 27241-120
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugTadalafil NDC 62332-177
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 62332-178
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 62332-179
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 62332-180
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan And Hydrochlorothiazide NDC 62332-209
- Generic Name
- Telmisartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan And Hydrochlorothiazide NDC 62332-210
- Generic Name
- Telmisartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan And Hydrochlorothiazide NDC 62332-211
- Generic Name
- Telmisartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugTadalafil NDC 46708-177
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 46708-178
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 46708-179
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 46708-180
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan And Hydrochlorothiazide NDC 46708-209
- Generic Name
- Telmisartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan And Hydrochlorothiazide NDC 46708-210
- Generic Name
- Telmisartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan And Hydrochlorothiazide NDC 46708-211
- Generic Name
- Telmisartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
American Health Packaging
NDC Product
Human Prescription DrugFenofibrate NDC 60687-853
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcyclovir NDC 60687-856
- Generic Name
- Acyclovir
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 60687-864
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcyclovir NDC 60687-867
- Generic Name
- Acyclovir
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugMucus Dm NDC 46122-420
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Pseudoephedrine Hcl NDC 46122-801
- Generic Name
- Guaifenesin And Pseudoephedrine Hcl
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugSymbicort NDC 0186-0370
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSymbicort NDC 0186-0372
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBudesonide And Formoterol Fumarate Dihydrate NDC 0310-7370
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugBudesonide And Formoterol Fumarate Dihydrate NDC 0310-7372
- Generic Name
- Budesonide And Formoterol Fumarate Dihydrate
- Dosage Form
- Aerosol
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugFenofibrate NDC 59651-201
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 59651-202
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 59651-203
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 59651-426
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 59651-427
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 59651-428
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTramadol Hydrochloride NDC 59651-441
- Generic Name
- Tramadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tramadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 59651-464
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 59651-465
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 59651-466
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 59651-467
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurohealth LLC
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 58602-714
- 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 58602-715
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 58602-810
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 58602-811
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 58602-824
- 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 58602-825
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Pseudoephedrine Hcl NDC 58602-833
- Generic Name
- Guaifenesin And Pseudoephedrine Hcl
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Pseudoephedrine Hcl NDC 58602-834
- Generic Name
- Guaifenesin And Pseudoephedrine Hcl
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 58602-849
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 58602-853
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 58602-864
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 58602-865
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 58602-871
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugLapatinib NDC 42291-035
- Generic Name
- Lapatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bayer HealthCare Pharmaceuticals Inc.
NDC Product
Human Prescription DrugYasmin NDC 50419-402
- Generic Name
- Drospirenone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNatazia NDC 50419-409
- Generic Name
- Estradiol Valerate And Estradiol Valerate/dienogest
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAngeliq NDC 50419-482
- Generic Name
- Drospirenone And Estradiol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAngeliq NDC 50419-483
- Generic Name
- Drospirenone And Estradiol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Better Living Brands LLC
NDC Product
Human Otc DrugGuaifenesin NDC 21130-179
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm Maximum Strength NDC 21130-989
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 21130-997
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Better Living Brands, LLC
NDC Product
Human Otc DrugMucus Relief Max NDC 21130-399
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Pharmacy, Inc.
NDC Product
Human Otc DrugMaximum Strength Cough And Congestion Extended Release NDC 51316-060
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCough And Congestion Extended Release NDC 51316-065
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugOmeprazole NDC 62135-559
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr.Reddys Laboratories Inc
NDC Product
Human Prescription DrugSunitinib Malate NDC 43598-045
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 43598-046
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 43598-047
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 43598-048
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugXofluza NDC 50242-860
- Generic Name
- Baloxavir Marboxil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugFenofibrate NDC 51407-093
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAcyclovir NDC 23155-227
- Generic Name
- Acyclovir
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcyclovir NDC 23155-228
- Generic Name
- Acyclovir
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcyclovir NDC 23155-229
- Generic Name
- Acyclovir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 0054-0254
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 0054-0255
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc DrugGuaifenesin And Pseudoephedrine Hcl NDC 30142-137
- Generic Name
- Guaifenesin And Pseudoephedrine Hcl
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 30142-275
- 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 30142-276
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugPramipexole Dihydrochloride NDC 33342-031
- Generic Name
- Pramipexole Dihydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPramipexole Dihydrochloride NDC 33342-032
- Generic Name
- Pramipexole Dihydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPramipexole Dihydrochloride NDC 33342-033
- Generic Name
- Pramipexole Dihydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPramipexole Dihydrochloride NDC 33342-034
- Generic Name
- Pramipexole Dihydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPramipexole Dihydrochloride NDC 33342-035
- Generic Name
- Pramipexole Dihydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7253
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7254
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7255
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcyclovir NDC 0904-7519
- Generic Name
- Acyclovir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugPrevymis NDC 0006-3075
- Generic Name
- Letermovir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-3076
- Generic Name
- Letermovir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-5003
- Generic Name
- Letermovir
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-5004
- Generic Name
- Letermovir
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Micro Labs Limited
NDC Product
Human Prescription DrugNevirapine NDC 42571-131
- Generic Name
- Nevirapine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugNorethindrone Acetate And Ethinyl Estradiol NDC 0378-7274
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNorethindrone Acetate And Ethinyl Estradiol NDC 0378-7280
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNorethindrone Acetate And Ethinyl Estradiol NDC 0378-7283
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Levonorgestrel And Ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevonorgestrel And Ethinyl Estradiol NDC 0378-7287
- Generic Name
- Levonorgestrel And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNorethindrone Acetate And Ethinyl Estradiol NDC 0378-7288
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesogestrel And Ethinyl Estradiol And Ethinyl Estradiol NDC 0378-7296
- Generic Name
- Desogestrel And Ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDrospirenone And Ethinyl Estradiol NDC 0378-7300
- Generic Name
- Drospirenone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEthynodiol Diacetate And Ethinyl Estradiol NDC 0378-7306
- Generic Name
- Ethynodiol Diacetate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEthynodiol Diacetate And Ethinyl Estradiol NDC 0378-7307
- Generic Name
- Ethynodiol Diacetate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Levonorgestrel And Ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBreyna NDC 0378-7502
- Generic Name
- Budesonide And Formoterol Fumarate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBreyna NDC 0378-7503
- Generic Name
- Budesonide And Formoterol Fumarate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugSpironolactone NDC 0615-8451
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 0615-8452
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugSpironolactone NDC 51655-344
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 51655-893
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSpironolactone NDC 43063-832
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 43063-835
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 43063-974
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Padagis US LLC
NDC Product
Human Prescription DrugBromocriptine Mesylate NDC 0574-0106
- Generic Name
- Bromocriptine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugBosulif NDC 0069-0135
- Generic Name
- Bosutinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBosulif NDC 0069-0136
- Generic Name
- Bosutinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBosulif NDC 0069-0193
- Generic Name
- Bosutinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0550
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0770
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0830
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0980
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
QPharma Inc
NDC Product
Human Prescription DrugOmeprazole NDC 42708-170
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 42708-180
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
RITE AID CORPORATION
NDC Product
Human Otc DrugGuaifenesin NDC 11822-4260
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rhodes Pharmaceuticals L.P.
NDC Product
Human Prescription DrugFenofibrate NDC 42858-067
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 42858-134
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 42858-200
- Generic Name
- Fenofibrate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 42858-454
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 42858-660
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugTramadol Hydrochloride NDC 16571-716
- Generic Name
- Tramadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 16571-773
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 16571-774
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 16571-775
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
ST. MARY'S MEDICAL PARK PHARMACY
NDC Product
Human Prescription DrugTramadol Hydrochloride NDC 60760-772
- Generic Name
- Tramadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlimepiride NDC 60760-800
- Generic Name
- Glimepiride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safecor Health LLC
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 48433-081
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2234
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2785
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2790
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2859
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2868
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol Valerate And Estradiol Valerate/dienogest NDC 0781-4110
- Generic Name
- Estradiol Valerate And Estradiol Valerate/dienogest
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
St. Mary's Medical Park Pharmacy
NDC Product
Human Prescription DrugOmeprazole NDC 60760-868
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Target Corporation
NDC Product
Human Otc DrugGuaifenesin And Dextromethorphan Hbr NDC 11673-267
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
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 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 DrugCimetidine NDC 0093-8305
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugLapatinib NDC 0480-3237
- Generic Name
- Lapatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
U.S. Pharmaceuticals
NDC Product
Human Prescription DrugSutent NDC 63539-017
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 63539-019
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBosulif NDC 63539-117
- Generic Name
- Bosutinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugGuaifenesin NDC 0363-0028
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0363-0033
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Pseudoephedrine Hcl NDC 0363-0134
- Generic Name
- Guaifenesin And Pseudoephedrine Hcl
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 0363-0474
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMaximum Strength Mucus Relief Dm NDC 0363-0510
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Pseudoephedrine Hcl NDC 0363-9946
- Generic Name
- Guaifenesin And Pseudoephedrine Hcl
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wal-Mart Stores, Inc.
NDC Product
Human Otc DrugMaximum Strength Mucus Relief Dm NDC 49035-956
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 49035-960
- Generic Name
- Guaifenesin And Dextromethorphan Hbr
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Whole Foods Market, Inc.
NDC Product
Human Otc Drug365 Whole Foods Market Guaifenesin NDC 42681-0057
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0841
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0843
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0844
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
