Product NDC: | 0025-1851 |
Proprietary Name: | CALAN |
Non Proprietary Name: | verapamil hydrochloride |
Active Ingredient(s): | 80 mg/1 & nbsp; verapamil hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0025-1851 |
Labeler Name: | G.D. Searle LLC Division of Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018817 |
Marketing Category: | NDA |
Start Marketing Date: | 19840910 |
Package NDC: | 0025-1851-52 |
Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (0025-1851-52) |
NDC Code | 0025-1851-52 |
Proprietary Name | CALAN |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (0025-1851-52) |
Product NDC | 0025-1851 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | verapamil hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19840910 |
Marketing Category Name | NDA |
Labeler Name | G.D. Searle LLC Division of Pfizer Inc |
Substance Name | VERAPAMIL HYDROCHLORIDE |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |