Hydroxyzine Hydrochloride
NDC 71335-3036, Hydroxyzine Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-3036
- 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/71335-3036 \ -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 |
|---|---|---|
| 71335-3036-1 | 71335303601 | 1000 TABLET, FILM COATED in 1 BOTTLE (71335-3036-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3526a66b-2182-4b5a-a7d1-563d75f5335f
Use it
Look up 71335-3036 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3036 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-3036. 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.