Benadryl
NDC 53209-3001, Diphenhydramine Hydrochloride, tablet, film coated, from Morning Star OTC.
- Product NDC
- 53209-3001
- Status
- Listed
- Labeler
- Morning Star OTC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M012
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/53209-3001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 53209-3001-2 | 53209300102 | 25 BLISTER PACK in 1 PACKET (53209-3001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-3001-1) |
Linked data
RxNorm, label and prices
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 53209-3001 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/53209-3001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 53209-3001. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.