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Metoprolol Tartrate
Metoprolol Tartrate - 13107-064-99 - (Metoprolol Tartrate)
Drug Information of Metoprolol Tartrate
| Product NDC: | 13107-064 |
| Proprietary Name: | Metoprolol Tartrate |
| Non Proprietary Name: | Metoprolol Tartrate |
| Active Ingredient(s): | 100 mg/1 & nbsp; Metoprolol Tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoprolol Tartrate
| Product NDC: | 13107-064 |
| Labeler Name: | Aurolife Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077739 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100917 |
Package Information of Metoprolol Tartrate
| Package NDC: | 13107-064-99 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (13107-064-99) |
NDC Information of Metoprolol Tartrate
| NDC Code | 13107-064-99 |
| Proprietary Name | Metoprolol Tartrate |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (13107-064-99) |
| Product NDC | 13107-064 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol Tartrate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100917 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurolife Pharma LLC |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
