Hydroxyzine Hydrochloride
NDC 72162-2511, Hydroxyzine Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 72162-2511
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA087871
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2511 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYZINE DIHYDROCHLORIDE10 mg/1
Pharmacologic classes
Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-2511-1 | 72162251101 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2511-1) |
| 72162-2511-5 | 72162251105 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2511-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7c959515-a5a9-4d5e-90e9-bd58bc947330
Use it
Look up 72162-2511 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2511 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-2511. 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.