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Verapamil
Verapamil - 60505-2741-5 - (Verapamil hydrochloride)
Drug Information of Verapamil
| Product NDC: | 60505-2741 |
| Proprietary Name: | Verapamil |
| Non Proprietary Name: | Verapamil hydrochloride |
| Active Ingredient(s): | 180 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
| Product NDC: | 60505-2741 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200878 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121119 |
Package Information of Verapamil
| Package NDC: | 60505-2741-5 |
| Package Description: | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-2741-5) |
NDC Information of Verapamil
| NDC Code | 60505-2741-5 |
| Proprietary Name | Verapamil |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-2741-5) |
| Product NDC | 60505-2741 |
| 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 | 20121119 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | VERAPAMIL HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
