Bisoprolol Fumarate
- Product NDC
- 68788-6775
- 11-digit product format
- 687886775
- Labeler code
- 68788
- Product ID
- 68788-6775_8529cb5e-2b92-4cdd-a84a-5ecb5fde44bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bisoprolol fumarate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078635
- Marketing category
- ANDA
- Marketing start
- 2016-10-24
- Marketing end
- 0000-00-00
- Substance
- BISOPROLOL FUMARATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record