NDC product
Extra Strength Pain Reliever
NDC 29485-9281 · Lil' Drug Store Products, Inc.
Key facts
| Product NDC | 29485-9281 |
|---|---|
| Proprietary name | Extra Strength Pain Reliever |
| Nonproprietary name | Acetaminophen 500 mg |
| Substances | ACETAMINOPHEN |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Lil' Drug Store Products, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M013 |
| Marketing start | Jan 17, 2017 |
| Marketing end | Jun 18, 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