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METOPROLOL SUCCINATE
METOPROLOL SUCCINATE - 68084-302-21 - (METOPROLOL SUCCINATE)
Drug Information of METOPROLOL SUCCINATE
| Product NDC: | 68084-302 |
| 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) |
Labeler Information of METOPROLOL SUCCINATE
| Product NDC: | 68084-302 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090615 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100813 |
Package Information of METOPROLOL SUCCINATE
| Package NDC: | 68084-302-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-302-21) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-302-11) |
NDC Information of METOPROLOL SUCCINATE
| NDC Code | 68084-302-21 |
| Proprietary Name | METOPROLOL SUCCINATE |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-302-21) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-302-11) |
| Product NDC | 68084-302 |
| 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 | 20100813 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
