NDC product
Bisoprolol
NDC 42571-471 · Micro Labs Limited
Key facts
| Product NDC | 42571-471 |
|---|---|
| Proprietary name | Bisoprolol |
| Nonproprietary name | Bisoprolol fumarate |
| Substances | BISOPROLOL FUMARATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Micro Labs Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA218303 |
| Pharmacologic classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| Marketing start | Jun 1, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: