Meclizine Hydrochloride
NDC 50268-522, Meclizine, tablet, from AvPAK.
- Product NDC
- 50268-522
- Status
- Listed
- Labeler
- AvPAK
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA201451
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50268-522 \ -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 |
|---|---|---|
| 50268-522-15 | 50268052215 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-522-15) / 1 TABLET in 1 BLISTER PACK (50268-522-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/af5d0c9b-a997-8033-afca-3c04221f2e76NADAC price for package 50268052215
GET /v1/drugs/nadac/50268052215
Use it
Look up 50268-522 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50268-522 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50268-522. 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.