Product NDC: | 64679-737 |
Proprietary Name: | METOPROLOL SUCCINATE |
Non Proprietary Name: | METOPROLOL SUCCINATE |
Active Ingredient(s): | 200 mg/1 & nbsp; METOPROLOL SUCCINATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64679-737 |
Labeler Name: | WOCKHARDT USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090615 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100722 |
Package NDC: | 64679-737-05 |
Package Description: | 10 BLISTER PACK in 1 CARTON (64679-737-05) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Code | 64679-737-05 |
Proprietary Name | METOPROLOL SUCCINATE |
Package Description | 10 BLISTER PACK in 1 CARTON (64679-737-05) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 64679-737 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METOPROLOL SUCCINATE |
Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20100722 |
Marketing Category Name | ANDA |
Labeler Name | WOCKHARDT USA LLC |
Substance Name | METOPROLOL SUCCINATE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |