NDC product
labetalol hydrochloride
NDC 25021-317 · Sagent Pharmaceuticals
Key facts
| Product NDC | 25021-317 |
|---|---|
| Proprietary name | labetalol hydrochloride |
| Nonproprietary name | labetalol hydrochloride |
| Substances | LABETALOL HYDROCHLORIDE |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Labeler | Sagent Pharmaceuticals |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA214533 |
| Pharmacologic classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| Marketing start | Sep 1, 2022 |
| Listing certified through | Dec 31, 2026 |
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: