NDC product
CEFAZOLIN
NDC 0404-9835 · Henry Schein Inc.
Key facts
| Product NDC | 0404-9835 |
|---|---|
| Proprietary name | CEFAZOLIN |
| Nonproprietary name | cefazolin |
| Substances | CEFAZOLIN SODIUM |
| Dosage form | INJECTION, POWDER, FOR SOLUTION |
| Route | INTRAMUSCULAR, INTRAVENOUS |
| Labeler | Henry Schein Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA065047 |
| Pharmacologic classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
| Marketing start | Jan 9, 2022 |
| Marketing end | Oct 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