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Meclizine Hydrochloride

NDC 70771-1539, Meclizine Hydrochloride, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1539
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1539 \
  -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 NDCNDC-11Package
70771-1539-0707711539001000 TABLET in 1 BOTTLE (70771-1539-0)
70771-1539-170771153901100 TABLET in 1 BOTTLE (70771-1539-1)
70771-1539-37077115390330 TABLET in 1 BOTTLE (70771-1539-3)
70771-1539-47077115390410 BLISTER PACK in 1 CARTON (70771-1539-4) / 10 TABLET in 1 BLISTER PACK (70771-1539-2)
70771-1539-97077115390990 TABLET in 1 BOTTLE (70771-1539-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cf157a71-f80a-4fb7-b892-7102b65a8ec0

Use it

Look up 70771-1539 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1539 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1539. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.