NDC product
Pain Relief PM Extra Strength
NDC 36800-095 · TopCo Associates LLC
Key facts
| Product NDC | 36800-095 |
|---|---|
| Proprietary name | Pain Relief PM |
| Nonproprietary name | Acetaminophen and Diphenhydramine Hydrochloride |
| Substances | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | TopCo Associates LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M013 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Nov 30, 2012 |
| Listing certified through | Dec 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 · Source date: