NDC product
Diphenhydramine HCL
NDC 66267-779 · NuCare Pharmaceuticals, Inc.
Key facts
| Product NDC | 66267-779 |
|---|---|
| Proprietary name | Diphenhydramine HCL |
| Nonproprietary name | Diphenhydramine HCL |
| Substances | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | NuCare Pharmaceuticals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Jan 27, 2010 |
| 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: