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Metoprolol Tartate
Metoprolol Tartate - 49349-438-02 - (Metoprolol Tartrate)
Drug Information of Metoprolol Tartate
| Product NDC: | 49349-438 |
| Proprietary Name: | Metoprolol Tartate |
| Non Proprietary Name: | Metoprolol Tartrate |
| Active Ingredient(s): | 100 mg/1 & nbsp; Metoprolol Tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoprolol Tartate
| Product NDC: | 49349-438 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074217 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110801 |
Package Information of Metoprolol Tartate
| Package NDC: | 49349-438-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-438-02) |
NDC Information of Metoprolol Tartate
| NDC Code | 49349-438-02 |
| Proprietary Name | Metoprolol Tartate |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-438-02) |
| Product NDC | 49349-438 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol Tartrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
