Meclizine HCl
NDC 57237-333, MECLIZINE HYDROCHLORIDE, tablet, from Rising Pharma Holdings, Inc..
- Product NDC
- 57237-333
- Status
- Listed
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M009.50
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/57237-333 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MECLIZINE HYDROCHLORIDE12.5 mg/1
Pharmacologic classes
Antiemetic [EPC]; Emesis Suppression [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57237-333-01 | 57237033301 | 100 TABLET in 1 BOTTLE (57237-333-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
NADAC price for package 57237033301
GET /v1/drugs/nadac/57237033301
Use it
Look up 57237-333 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57237-333 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57237-333. 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.