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METOPROLOL TARTRATE
METOPROLOL TARTRATE - 60760-251-60 - (METOPROLOL TARTRATE)
Drug Information of METOPROLOL TARTRATE
| Product NDC: | 60760-251 |
| Proprietary Name: | METOPROLOL TARTRATE |
| Non Proprietary Name: | METOPROLOL TARTRATE |
| Active Ingredient(s): | 50 mg/1 & nbsp; METOPROLOL TARTRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METOPROLOL TARTRATE
| Product NDC: | 60760-251 |
| Labeler Name: | St Marys Medical Park Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074644 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130515 |
Package Information of METOPROLOL TARTRATE
| Package NDC: | 60760-251-60 |
| Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (60760-251-60) |
NDC Information of METOPROLOL TARTRATE
| NDC Code | 60760-251-60 |
| Proprietary Name | METOPROLOL TARTRATE |
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (60760-251-60) |
| Product NDC | 60760-251 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METOPROLOL TARTRATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130515 |
| Marketing Category Name | ANDA |
| Labeler Name | St Marys Medical Park Pharmacy |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
