Product NDC: | 49999-226 |
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) |
Product NDC: | 49999-226 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078459 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120316 |
Package NDC: | 49999-226-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (49999-226-60) |
NDC Code | 49999-226-60 |
Proprietary Name | Metoprolol Tartrate |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (49999-226-60) |
Product NDC | 49999-226 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metoprolol Tartrate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120316 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | METOPROLOL TARTRATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |