Hydroxyzine Hydrochloride
NDC 71656-090, Hydroxyzine Hydrochloride, solution, from Saptalis Pharmaceuticals, LLC..
- Product NDC
- 71656-090
- Status
- Listed
- Labeler
- Saptalis Pharmaceuticals, LLC.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA220271
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71656-090 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYZINE HYDROCHLORIDE10 mg/5mL
Pharmacologic classes
Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71656-090-16 | 71656009016 | 473 mL in 1 BOTTLE (71656-090-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9ab23881-334c-474d-9d93-25ea225548dc
Use it
Look up 71656-090 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71656-090 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71656-090. 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.