Product NDC: | 24236-428 |
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, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24236-428 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076704 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130318 |
Package NDC: | 24236-428-10 |
Package Description: | 6 TABLET, FILM COATED in 1 BLISTER PACK (24236-428-10) |
NDC Code | 24236-428-10 |
Proprietary Name | Metoprolol Tartrate |
Package Description | 6 TABLET, FILM COATED in 1 BLISTER PACK (24236-428-10) |
Product NDC | 24236-428 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metoprolol tartrate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130318 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | METOPROLOL TARTRATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |