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MECLIZINE HYDROCHLORIDE

NDC 71335-3157, MECLIZINE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3157
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202640
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3157 \
  -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 NDCNDC-11Package
71335-3157-07133531570014 TABLET in 1 BOTTLE (71335-3157-0)
71335-3157-17133531570190 TABLET in 1 BOTTLE (71335-3157-1)
71335-3157-27133531570230 TABLET in 1 BOTTLE (71335-3157-2)
71335-3157-37133531570325 TABLET in 1 BOTTLE (71335-3157-3)
71335-3157-47133531570420 TABLET in 1 BOTTLE (71335-3157-4)
71335-3157-57133531570540 TABLET in 1 BOTTLE (71335-3157-5)
71335-3157-67133531570660 TABLET in 1 BOTTLE (71335-3157-6)
71335-3157-771335315707120 TABLET in 1 BOTTLE (71335-3157-7)
71335-3157-87133531570810 TABLET in 1 BOTTLE (71335-3157-8)
71335-3157-971335315709100 TABLET in 1 BOTTLE (71335-3157-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dab43efd-bec6-472f-b13a-1c043914dcd1

Use it

Look up 71335-3157 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3157 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3157. 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.