NDC product
acetaminophen pain reliever fever reducer
NDC 45802-730 · Padagis Israel Pharmaceuticals Ltd
Key facts
| Product NDC | 45802-730 |
|---|---|
| Proprietary name | acetaminophen |
| Nonproprietary name | Acetaminophen |
| Substances | ACETAMINOPHEN |
| Dosage form | SUPPOSITORY |
| Route | RECTAL |
| Labeler | Padagis Israel Pharmaceuticals Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA070608 |
| Marketing start | Oct 28, 2010 |
| Marketing end | Nov 30, 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