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METOPROLOL SUCCINATE
METOPROLOL SUCCINATE - 55648-736-09 - (METOPROLOL SUCCINATE)
Drug Information of METOPROLOL SUCCINATE
| Product NDC: | 55648-736 |
| Proprietary Name: | METOPROLOL SUCCINATE |
| Non Proprietary Name: | METOPROLOL SUCCINATE |
| Active Ingredient(s): | 100 mg/1 & nbsp; METOPROLOL SUCCINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METOPROLOL SUCCINATE
| Product NDC: | 55648-736 |
| Labeler Name: | WOCKHARDT LIMITED |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090615 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100722 |
Package Information of METOPROLOL SUCCINATE
| Package NDC: | 55648-736-09 |
| Package Description: | 12 BOTTLE in 1 CARTON (55648-736-09) > 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of METOPROLOL SUCCINATE
| NDC Code | 55648-736-09 |
| Proprietary Name | METOPROLOL SUCCINATE |
| Package Description | 12 BOTTLE in 1 CARTON (55648-736-09) > 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 55648-736 |
| 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 LIMITED |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
