bisoprolol fumarate
- Product NDC
- 0185-0771
- 11-digit product format
- 001850771
- Labeler code
- 0185
- Product ID
- 0185-0771_15d8ea4a-9105-46af-9b44-7ea7726c3691
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bisoprolol fumarate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA075643
- Marketing category
- ANDA
- Marketing start
- 2000-11-16
- Marketing end
- 2021-09-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0185-0771-01 | 00185077101 | 100 TABLET, COATED in 1 BOTTLE (0185-0771-01) | 2000-11-16 | 2021-09-30 | No | No | Current |
| 0185-0771-30 | 00185077130 | 30 TABLET, COATED in 1 BOTTLE (0185-0771-30) | 2000-11-16 | 2021-08-31 | No | No | Current |