NDC product
IBUPROFEN
NDC 29485-9291 · Lil' Drug Store Products, Inc.
Key facts
| Product NDC | 29485-9291 |
|---|---|
| Proprietary name | IBUPROFEN |
| Nonproprietary name | IBUPROFEN 200MG |
| Substances | IBUPROFEN |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Lil' Drug Store Products, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA075010 |
| Pharmacologic classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| Marketing start | May 2, 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