Product NDC: | 16252-540 |
Proprietary Name: | Isradipine |
Non Proprietary Name: | Isradipine |
Active Ingredient(s): | 5 mg/1 & nbsp; Isradipine |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16252-540 |
Labeler Name: | Cobalt Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077317 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060105 |
Package NDC: | 16252-540-01 |
Package Description: | 100 CAPSULE in 1 BOTTLE (16252-540-01) |
NDC Code | 16252-540-01 |
Proprietary Name | Isradipine |
Package Description | 100 CAPSULE in 1 BOTTLE (16252-540-01) |
Product NDC | 16252-540 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Isradipine |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20060105 |
Marketing Category Name | ANDA |
Labeler Name | Cobalt Laboratories |
Substance Name | ISRADIPINE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |