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verapamil hydrochloride
verapamil hydrochloride - 68462-260-01 - (verapamil hydrochloride)
Drug Information of verapamil hydrochloride
| Product NDC: | 68462-260 |
| Proprietary Name: | verapamil hydrochloride |
| Non Proprietary Name: | verapamil hydrochloride |
| Active Ingredient(s): | 240 mg/1 & nbsp; verapamil hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of verapamil hydrochloride
| Product NDC: | 68462-260 |
| Labeler Name: | Glenmark Generics Inc.,USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078906 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090917 |
Package Information of verapamil hydrochloride
| Package NDC: | 68462-260-01 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-01) |
NDC Information of verapamil hydrochloride
| NDC Code | 68462-260-01 |
| Proprietary Name | verapamil hydrochloride |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-01) |
| Product NDC | 68462-260 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | verapamil hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090917 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc.,USA |
| Substance Name | VERAPAMIL HYDROCHLORIDE |
| Strength Number | 240 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
