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: | 54868-6124-0 |
Package Description: | 10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-6124-0) |
NDC Code | 54868-6124-0 |
Proprietary Name | Verapamil Hydrochloride |
Package Description | 10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-6124-0) |
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] |