NDC product
TABLET, FILM COATED · Teva Pharmaceuticals USA, Inc.
NDC 16252-514 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 16252-514 |
|---|---|
| Nonproprietary name | Ciprofloxacin |
| Substances | CIPROFLOXACIN HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | DRUG FOR FURTHER PROCESSING |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| Marketing start | Jun 9, 2004 |
| Marketing end | Aug 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