Hydroxyzine Hydrochloride
NDC 72789-269, Hydroxyzine Hydrochloride, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-269
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA088619
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-269 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYZINE DIHYDROCHLORIDE50 mg/1
Pharmacologic classes
Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72789-269-30 | 72789026930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-269-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/214b3f14-2f6c-4f36-b7a6-e0b1f820e3a7
Use it
Look up 72789-269 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-269 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-269. 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.