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
Substance Identification & Data
This profile provides standardized clinical and technical data for Microcrystalline Cellulose 102, uniquely identified by the FDA Unique Ingredient Identifier (UNII) PNR0YF693Y.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-34-6 and the RxNorm Concept ID (RxCUI) 2056923. 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 102
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
PNR0YF693Y
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 102. 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 102
CN
CELLULOSE, MICROCRYSTALLINE PH102
CN
CELLULOSE, MICROCRYSTALLINE PH102 [II]
CN
MICROCRYSTALLINE CELLULOSE 102
CN
MICROCRYSTALLINE CELLULOSE 102 IS INCLUDED IN FDA INACTIVE INGREDIENTS AS MICROCRYSTALLINE CELLULOSE
CN
Brand / Trade Names
AVICEL PH 102
BN
AVICEL PH-102
BN
CEOLUS PH-102
BN
VIVAPUR 102
BN
VIVAPUR MCC SPHERES - GRADE 100
BN
VIVAPUR PH-102
BN
NDC Products Containing MICROCRYSTALLINE CELLULOSE 102
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 DrugCyclobenzaprine Hydrochloride NDC 50090-5711
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 50090-5712
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 50090-5713
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 50090-5756
- Generic Name
- Cyclobenzaprine Hydrochloride
- 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
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugCaptopril NDC 11788-135
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 11788-136
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 11788-137
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 11788-138
- Generic Name
- Captopril
- Dosage Form
- Tablet
- 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
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugSevelamer Carbonate NDC 0115-1365
- Generic Name
- Sevelamer Carbonate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSevelamer Carbonate NDC 0115-1366
- Generic Name
- Sevelamer Carbonate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugAzithromycin NDC 42291-044
- Generic Name
- Azithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-908
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-909
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-910
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-911
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-912
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
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
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 DrugMesalamine NDC 31722-043
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, 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 DrugTeriflunomide NDC 31722-246
- Generic Name
- Teriflunomide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTeriflunomide NDC 31722-247
- Generic Name
- Teriflunomide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImatinib Mesylate NDC 31722-296
- Generic Name
- Imatinib Mesylate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImatinib Mesylate NDC 31722-297
- Generic Name
- Imatinib Mesylate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEletriptan Hydrobromide NDC 31722-443
- Generic Name
- Eletriptan Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEletriptan Hydrobromide NDC 31722-444
- Generic Name
- Eletriptan Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-445
- Generic Name
- Amlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-446
- Generic Name
- Aamlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-447
- Generic Name
- Amlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-448
- Generic Name
- Amlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 31722-487
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 31722-488
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEmtricitabine And Tenofovir Disoproxil Fumarate NDC 31722-560
- Generic Name
- Emtricitabine And Tenofovir Disoproxil Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 31722-585
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 31722-586
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 31722-587
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 31722-588
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRoflumilast NDC 31722-623
- Generic Name
- Roflumilast
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPosaconazole NDC 31722-677
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextromethorphan Hydrobromide And Quinidine Sulfate NDC 31722-693
- Generic Name
- Dextromethorphan Hydrobromide And Quinidine Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 31722-805
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 31722-806
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- 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 DrugEszopiclone NDC 31722-855
- Generic Name
- Eszopiclone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEszopiclone NDC 31722-856
- Generic Name
- Eszopiclone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEszopiclone NDC 31722-857
- Generic Name
- Eszopiclone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolvaptan NDC 31722-869
- Generic Name
- Tolvaptan
- Dosage Form
- Tablet
- 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 DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 31722-892
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 31722-893
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 31722-894
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 31722-895
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 31722-896
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugColchicine NDC 31722-899
- Generic Name
- Colchicine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy's Laboratories Inc.
NDC Product
Human Prescription DrugSacubitril And Valsartan Sacubitril And Valsartan NDC 43598-643
- Generic Name
- Sacubitril And Valsartan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSacubitril And Valsartan Sacubitril And Valsartan NDC 43598-644
- Generic Name
- Sacubitril And Valsartan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSacubitril And Valsartan Sacubitril And Valsartan NDC 43598-645
- Generic Name
- Sacubitril And Valsartan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugIsosorbide Dinitrate NDC 49884-556
- Generic Name
- Isosorbide Dinitrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 23155-832
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 23155-833
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 23155-834
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 23155-835
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Valsartan NDC 23155-844
- Generic Name
- Amlodipine And Valsartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Valsartan NDC 23155-845
- Generic Name
- Amlodipine And Valsartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Valsartan NDC 23155-846
- Generic Name
- Amlodipine And Valsartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Valsartan NDC 23155-847
- Generic Name
- Amlodipine And Valsartan
- 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
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 Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4661
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4662
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4663
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4664
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4665
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4666
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4667
- Generic Name
- Lisdexamfetamine Dimesylate
- 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 DrugFamotidine 10 Mg NDC 25000-086
- Generic Name
- Famotidine 10 Mg
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugFamotidine 20 Mg NDC 25000-087
- Generic Name
- Famotidine 20 Mg
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugFamotidine 20 Mg NDC 25000-124
- Generic Name
- Famotidine 20 Mg
- Dosage Form
- Tablet, Coated
- 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
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 0904-7447
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 0904-7448
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 0904-7449
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydralazine Hydrochloride NDC 0904-7450
- Generic Name
- Hydralazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
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 DrugLisdexamfetamine Dimesylate NDC 0378-6854
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0378-6855
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0378-6856
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0378-6857
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0378-6858
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0378-6859
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0378-6860
- Generic Name
- Lisdexamfetamine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugPrednisone NDC 0615-8439
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0615-8440
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0615-8441
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0615-8508
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCiprofloxacin NDC 0615-8630
- Generic Name
- Ciprofloxacin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar RxLLC
NDC Product
Human Prescription DrugPosaconazole NDC 16714-535
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC
NDC Product
Human Prescription DrugChlorpromazine Hydrochloride NDC 16714-047
- Generic Name
- Chlorpromazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine Hydrochloride NDC 16714-048
- Generic Name
- Chlorpromazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine Hydrochloride NDC 16714-049
- Generic Name
- Chlorpromazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine Hydrochloride NDC 16714-050
- Generic Name
- Chlorpromazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine Hydrochloride NDC 16714-051
- Generic Name
- Chlorpromazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
QPharma, Inc.
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
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-161
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-162
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-163
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-164
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-165
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-166
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 42858-167
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- 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 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 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 DrugIndapamide NDC 16571-875
- Generic Name
- Indapamide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIndapamide NDC 16571-876
- Generic Name
- Indapamide
- Dosage Form
- Tablet
- 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 DrugMirtazapine NDC 48433-076
- Generic Name
- Mirtazapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMirtazapine NDC 48433-077
- Generic Name
- Mirtazapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMirtazapine NDC 48433-078
- Generic Name
- Mirtazapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Shandong New Time Pharmaceutical Co., Ltd.
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 42677-307
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugMaximum Strength Acid Reducer NDC 11673-697
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
TIME CAP LABORATORIES, INC.
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
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
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
NDC Product
Human Prescription DrugSorafenib NDC 0480-5425
- Generic Name
- Sorafenib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Tris Pharma Inc
NDC Product
Human Prescription DrugPregabalin NDC 27808-235
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 27808-236
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 27808-237
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 27808-238
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 27808-239
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 27808-240
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 27808-241
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugPrasugrel NDC 29300-301
- Generic Name
- Prasugrel
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrasugrel NDC 29300-302
- Generic Name
- Prasugrel
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol Hydrochloride NDC 29300-375
- Generic Name
- Nebivolol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol Hydrochloride NDC 29300-376
- Generic Name
- Nebivolol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol Hydrochloride NDC 29300-377
- Generic Name
- Nebivolol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol Hydrochloride NDC 29300-378
- Generic Name
- Nebivolol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 29300-382
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 29300-413
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 29300-414
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 29300-415
- Generic Name
- Cyclobenzaprine Hydrochloride
- 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
