Product NDC: | 23155-027 |
Proprietary Name: | Verapamil Hydrochloride |
Non Proprietary Name: | Verapamil Hydrochloride |
Active Ingredient(s): | 120 mg/1 & nbsp; Verapamil Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 23155-027 |
Labeler Name: | Heritage Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071881 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110107 |
Package NDC: | 23155-027-05 |
Package Description: | 500 TABLET in 1 BOTTLE (23155-027-05) |
NDC Code | 23155-027-05 |
Proprietary Name | Verapamil Hydrochloride |
Package Description | 500 TABLET in 1 BOTTLE (23155-027-05) |
Product NDC | 23155-027 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Verapamil Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110107 |
Marketing Category Name | ANDA |
Labeler Name | Heritage Pharmaceuticals Inc. |
Substance Name | VERAPAMIL HYDROCHLORIDE |
Strength Number | 120 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |