Home
>
National Drug Code (NDC)
>
Verapamil Hydrochloride
Verapamil Hydrochloride - 52125-123-02 - (verapamil hydrochloride)
Drug Information of Verapamil Hydrochloride
| Product NDC: | 52125-123 |
| Proprietary Name: | Verapamil Hydrochloride |
| 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 Hydrochloride
| Product NDC: | 52125-123 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074587 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130314 |
Package Information of Verapamil Hydrochloride
| Package NDC: | 52125-123-02 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-123-02) |
NDC Information of Verapamil Hydrochloride
| NDC Code | 52125-123-02 |
| Proprietary Name | Verapamil Hydrochloride |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-123-02) |
| Product NDC | 52125-123 |
| 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 | 20130314 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | VERAPAMIL HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
