Meclizine Hydrochloride
NDC 71335-1872, Meclizine Hydrochloride, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-1872
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- 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/71335-1872 \ -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 |
|---|---|---|
| 71335-1872-1 | 71335187201 | 30 TABLET in 1 BOTTLE (71335-1872-1) |
| 71335-1872-2 | 71335187202 | 60 TABLET in 1 BOTTLE (71335-1872-2) |
| 71335-1872-3 | 71335187203 | 90 TABLET in 1 BOTTLE (71335-1872-3) |
| 71335-1872-4 | 71335187204 | 28 TABLET in 1 BOTTLE (71335-1872-4) |
| 71335-1872-5 | 71335187205 | 20 TABLET in 1 BOTTLE (71335-1872-5) |
| 71335-1872-6 | 71335187206 | 120 TABLET in 1 BOTTLE (71335-1872-6) |
| 71335-1872-7 | 71335187207 | 100 TABLET in 1 BOTTLE (71335-1872-7) |
| 71335-1872-8 | 71335187208 | 10 TABLET in 1 BOTTLE (71335-1872-8) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/112103bc-25e2-42cf-8542-ba1d3392a2c3
Use it
Look up 71335-1872 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1872 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-1872. 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.