Bisoprolol Fumarate
- Product NDC
- 68071-1582
- 11-digit product format
- 680711582
- Labeler code
- 68071
- Product ID
- 68071-1582_bb12153e-96dc-8c38-e053-2a95a90a5400
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bisoprolol fumarate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078635
- Marketing category
- ANDA
- Marketing start
- 2009-09-21
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1582-3 | 68071158203 | 30 TABLET in 1 BOTTLE (68071-1582-3) | 30 tablet | 2019-03-15 | 0000-00-00 | No | No | Current |