Product NDC: | 54868-0120 |
Proprietary Name: | Verapamil Hydrochloride |
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: | 54868-0120 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070995 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950424 |
Package NDC: | 54868-0120-2 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0120-2) |
NDC Code | 54868-0120-2 |
Proprietary Name | Verapamil Hydrochloride |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0120-2) |
Product NDC | 54868-0120 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Verapamil Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19950424 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | VERAPAMIL HYDROCHLORIDE |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |