NDC product
Ibuprofen PM
NDC 63868-829 · CHAIN DRUG MARKETING ASSOCIATION INC.
Key facts
| Product NDC | 63868-829 |
|---|---|
| Proprietary name | Ibuprofen PM |
| Nonproprietary name | IBUPROFEN, DIPHENHYDRAMINE HCL |
| Substances | IBUPROFEN, DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage form | CAPSULE, LIQUID FILLED |
| Route | ORAL |
| Labeler | CHAIN DRUG MARKETING ASSOCIATION INC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA090397 |
| Pharmacologic classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC] |
| Marketing start | Jun 11, 2021 |
| Listing certified through | Dec 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 · Source date: