Hydroxyzine Hydrochloride
NDC 60687-675, Hydroxyzine Hydrochloride, tablet, film coated, from American Health Packaging.
- Product NDC
- 60687-675
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA088618
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60687-675 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYZINE HYDROCHLORIDE25 mg/1
Pharmacologic classes
Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-675-01 | 60687067501 | 100 BLISTER PACK in 1 CARTON (60687-675-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-675-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/47bda4fe-ddb7-4140-900a-970373cc7accNADAC price for package 60687067501
GET /v1/drugs/nadac/60687067501
Use it
Look up 60687-675 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-675 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-675. 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.