NDC product
Buspirone Hydrochloride
NDC 0093-5200 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-5200 |
|---|---|
| Proprietary name | Buspirone Hydrochloride |
| Nonproprietary name | Buspirone Hydrochloride |
| Substances | BUSPIRONE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA075022 |
| Marketing start | Mar 26, 2004 |
| 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: