Meclizine Hydrochloride
NDC 72189-237, Meclizine Hydrochloride, tablet, from Direct_Rx.
- Product NDC
- 72189-237
- Status
- Listed
- Labeler
- Direct_Rx
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA010721
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72189-237 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MECLIZINE HYDROCHLORIDE25 mg/1
Pharmacologic classes
Antiemetic [EPC]; Emesis Suppression [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72189-237-30 | 72189023730 | 30 TABLET in 1 BOTTLE (72189-237-30) |
| 72189-237-90 | 72189023790 | 90 TABLET in 1 BOTTLE (72189-237-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e79ecf77-0e0a-d7ef-e053-2a95a90a5adf
Use it
Look up 72189-237 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72189-237 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72189-237. 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.