NDC Product
Human Prescription DrugDiclofenac Sodium NDC 50090-0540
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Microcrystalline Cellulose 101, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 7T9FYH5QMK.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-34-6 and the RxNorm Concept ID (RxCUI) 2058847. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
MICROCRYSTALLINE CELLULOSE 101
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
7T9FYH5QMK
The specific atomic composition represented as a molecular structure string.
Substance Type
specifiedSubstanceG1
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Microcrystalline Cellulose 101. 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
CELLULOSE, MICROCRYSTALLINE 101
CN
CELLULOSE, MICROCRYSTALLINE 101 [II]
CN
CELLULOSE, MICROCRYSTALLINE PH101
CN
CELLULOSE, MICROCRYSTALLINE PH101 [II]
CN
MICROCRYSTALLINE CELLULOSE 101
CN
MICROCRYSTALLINE CELLULOSE 101 IS INCLUDED IN FDA INACTIVE INGREDIENTS AS MICROCRYSTALLINE CELLULOSE
CN
Brand / Trade Names
AVICEL PH 101
BN
AVICEL PH-101
BN
CEOLUS PH-101
BN
VIVAPUR 101
BN
VIVAPUR PH-101
BN
NDC Products Containing MICROCRYSTALLINE CELLULOSE 101
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 DrugDiclofenac Sodium NDC 50090-0541
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5181
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5182
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5184
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5207
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5208
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeloxicam NDC 50090-5339
- Generic Name
- Meloxicam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeloxicam NDC 50090-5340
- Generic Name
- Meloxicam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 50090-5402
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-5433
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-5435
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-5444
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-5445
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-5446
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 50090-5918
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarisoprodol NDC 50090-5953
- Generic Name
- Carisoprodol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarisoprodol NDC 50090-5955
- Generic Name
- Carisoprodol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-6061
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 50090-6156
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 50090-6157
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 50090-6158
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 50090-6160
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-6369
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-6458
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-6539
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-6600
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-6676
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-6677
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClonidine Hydrochloride NDC 50090-6744
- Generic Name
- Clonidine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-6790
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 50090-6886
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiclofenac Sodium NDC 50090-6924
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-7178
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-7180
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-7196
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7358
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7359
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7384
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7385
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7386
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7387
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-7490
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-7491
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-7492
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-7493
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeloxicam NDC 50090-7495
- Generic Name
- Meloxicam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7528
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7529
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7532
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7533
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7574
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7575
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-7583
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-7598
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEzetimibe NDC 50090-7689
- Generic Name
- Ezetimibe
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEzetimibe NDC 50090-7690
- Generic Name
- Ezetimibe
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 50090-7797
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7806
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7807
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Accord Healthcare Inc.
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 16729-366
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 16729-367
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 16729-368
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amerisource Bergen
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
Aurohealth LLC
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 58602-760
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
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 DrugLoperamide Hydrochloride And Simethicone NDC 58602-815
- Generic Name
- Loperamide Hydrochloride And Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Naproxen Sodium And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Azurity Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugWidaplik NDC 24338-001
- Generic Name
- Telmisartan, Amlodipine And Indapamide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugWidaplik NDC 24338-002
- Generic Name
- Telmisartan, Amlodipine And Indapamide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugWidaplik NDC 24338-003
- Generic Name
- Telmisartan, Amlodipine And Indapamide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
BETTER LIVING BRANDS, LLC
NDC Product
Human Otc DrugLoratadine 10mg NDC 21130-932
- Generic Name
- Loratadine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
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
Better Living Brands, LLC
NDC Product
Human Otc DrugLoperamide Hydrochloride And Simethicone NDC 21130-222
- Generic Name
- Loperamide Hydrochloride And Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 21130-224
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
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
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 Health Corp
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFamotidine NDC 31722-017
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 31722-018
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 31722-021
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 31722-022
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDeferasirox NDC 31722-030
- Generic Name
- Deferasirox
- Dosage Form
- Granule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDeferasirox NDC 31722-031
- Generic Name
- Deferasirox
- Dosage Form
- Granule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 31722-032
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEplerenone NDC 31722-049
- Generic Name
- Eplerenone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEplerenone NDC 31722-050
- Generic Name
- Eplerenone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 31722-384
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 31722-385
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 31722-386
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 31722-387
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 31722-489
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPomalidomide NDC 31722-770
- Generic Name
- Pomalidomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPomalidomide NDC 31722-771
- Generic Name
- Pomalidomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPomalidomide NDC 31722-772
- Generic Name
- Pomalidomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPomalidomide NDC 31722-773
- Generic Name
- Pomalidomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-841
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-842
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-843
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-844
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-846
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-847
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-848
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-849
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil NDC 31722-852
- Generic Name
- Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil NDC 31722-853
- Generic Name
- Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil NDC 31722-854
- Generic Name
- Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 31722-879
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-880
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 31722-886
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 31722-887
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 31722-888
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Family Dollar Stores, LLC
NDC Product
Human Otc DrugLoperamide Hydrochloride And Simethicone NDC 55319-052
- Generic Name
- Loperamide Hydrochloride And Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 51407-379
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 51407-380
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 51407-381
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 51407-483
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 51407-484
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 51407-485
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 51407-921
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 51407-922
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 51407-923
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugVigabatrin NDC 0054-0652
- Generic Name
- Vigabatrin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 30142-058
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 30142-193
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
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
Kroger Company
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
MARKSANS PHARMA LIMITED
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 DrugAmitriptyline Hydrochloride NDC 0904-7410
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 0904-7411
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Medsource Pharmaceuticals
NDC Product
Human Prescription DrugCarisoprodol NDC 45865-233
- Generic Name
- Carisoprodol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Micro Labs Limited
NDC Product
Human Prescription DrugFenofibric Acid NDC 42571-347
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 42571-348
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugSorafenib Tosylate NDC 0378-1201
- Generic Name
- Sorafenib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0378-4500
- Generic Name
- Budesonide
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Emtricitabine, Rilpivirine, Tenofovir Disoproxil Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugCiprofloxacin NDC 0615-8630
- Generic Name
- Ciprofloxacin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar Rx LLC
NDC Product
Human Prescription DrugCarbidopa NDC 16714-067
- Generic Name
- Carbidopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 51655-088
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugValsartan NDC 51655-244
- Generic Name
- Valsartan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-464
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-465
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-747
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 51655-935
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
QPharma, Inc.
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-141
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-144
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCiprofloxacin NDC 42708-188
- Generic Name
- Ciprofloxacin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- 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 DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-721
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-722
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-723
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-724
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-725
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-726
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 42858-727
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rising Pharma Holdings, Inc
NDC Product
Human Prescription DrugBumetanide NDC 16571-677
- Generic Name
- Bumetanide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBumetanide NDC 16571-678
- Generic Name
- Bumetanide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBumetanide NDC 16571-679
- Generic Name
- Bumetanide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 16571-105
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 16571-106
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 16571-107
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 16571-108
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 16571-109
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 16571-110
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 16571-157
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 16571-158
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 16571-159
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProbenecid NDC 16571-831
- Generic Name
- Probenecid
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProbenecid And Colchicine NDC 16571-832
- Generic Name
- Probenecid And Colchicine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPentoxifylline NDC 16571-856
- Generic Name
- Pentoxifylline
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugFexofenadine Hydrochloride And Pseudoephedrine Hydrochloride NDC 11822-0021
- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safecor Health LLC
NDC Product
Human Prescription DrugLevetiracetam NDC 48433-052
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethotrexate NDC 48433-065
- Generic Name
- Methotrexate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugValacyclovir Hydrochloride NDC 48433-144
- Generic Name
- Valacyclovir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safecor Health, LLC
NDC Product
Human Prescription DrugClozapine NDC 48433-022
- Generic Name
- Clozapine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
TAGI Pharma, Inc.
NDC Product
Human Prescription DrugChlorthalidone NDC 51224-018
- Generic Name
- Chlorthalidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorthalidone NDC 51224-118
- Generic Name
- Chlorthalidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
TIME CAP LABORATORIES, INC.
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
Drug For Further Processing- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 0093-5571
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 0093-5572
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugFinzala NDC 0093-8210
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDasatinib NDC 0480-3523
- Generic Name
- Dasatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDasatinib NDC 0480-3524
- Generic Name
- Dasatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDasatinib NDC 0480-5101
- Generic Name
- Dasatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDasatinib NDC 0480-5102
- Generic Name
- Dasatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDasatinib NDC 0480-5103
- Generic Name
- Dasatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDasatinib NDC 0480-5104
- Generic Name
- Dasatinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
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 DrugCetirizine Hydrochloride NDC 0363-0471
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Cetirizine Hydrochloride NDC 0363-4025
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugLoperamide Hydrochloride And Simethicone NDC 0363-9606
- Generic Name
- Loperamide Hydrochloride And Simethicone
- Dosage Form
- Tablet
- 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
Walgreens Company
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- 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
