| Product NDC: | 54868-6124 |
| Proprietary Name: | Verapamil Hydrochloride |
| Non Proprietary Name: | verapamil hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; verapamil hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-6124 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078306 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100517 |
| Package NDC: | 54868-6124-1 |
| Package Description: | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-6124-1) |
| NDC Code | 54868-6124-1 |
| Proprietary Name | Verapamil Hydrochloride |
| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-6124-1) |
| Product NDC | 54868-6124 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | verapamil hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100517 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | VERAPAMIL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |