bisoprolol fumarate
- Product NDC
- 68084-487
- 11-digit product format
- 680840487
- Labeler code
- 68084
- Product ID
- 68084-487_7018ae1b-fb92-5669-e053-2a91aa0a2cc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bisoprolol fumarate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075643
- Marketing category
- ANDA
- Marketing start
- 2011-10-04
- Marketing end
- 2019-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record