NDC Code | 66993-475-02 |
Package Description | 1 BOTTLE in 1 CARTON (66993-475-02) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
Product NDC | 66993-475 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Nisoldipine |
Non-Proprietary Name | Nisoldipine |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20120227 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA020356 |
Manufacturer | Prasco Laboratories |
Substance Name | NISOLDIPINE |
Strength | 34 |
Strength Unit | mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |