MECLIZINE HYDROCHLORIDE
NDC 59746-121, Meclizine Hydrocloride, tablet, from Jubilant Cadista Pharmacuticals Inc..
- Product NDC
- 59746-121
- Status
- Listed
- Labeler
- Jubilant Cadista Pharmacuticals Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040659
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59746-121 \ -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 |
|---|---|---|
| 59746-121-06 | 59746012106 | 100 TABLET in 1 BOTTLE (59746-121-06) |
| 59746-121-10 | 59746012110 | 1000 TABLET in 1 BOTTLE (59746-121-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9350fefc-9c00-182c-c3a9-044d4a40856f
Use it
Look up 59746-121 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59746-121 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59746-121. 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.