Product NDC: | 0185-0771 |
Proprietary Name: | bisoprolol fumarate |
Non Proprietary Name: | bisoprolol fumarate |
Active Ingredient(s): | 5 mg/1 & nbsp; bisoprolol fumarate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0185-0771 |
Labeler Name: | Eon Labs, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075643 |
Marketing Category: | ANDA |
Start Marketing Date: | 20001116 |
Package NDC: | 0185-0771-30 |
Package Description: | 30 TABLET, COATED in 1 BOTTLE (0185-0771-30) |
NDC Code | 0185-0771-30 |
Proprietary Name | bisoprolol fumarate |
Package Description | 30 TABLET, COATED in 1 BOTTLE (0185-0771-30) |
Product NDC | 0185-0771 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | bisoprolol fumarate |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20001116 |
Marketing Category Name | ANDA |
Labeler Name | Eon Labs, Inc. |
Substance Name | BISOPROLOL FUMARATE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |