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Meclizine Hydrochloride

NDC 71610-836, Meclizine Hydrochloride, tablet, chewable, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-836
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, CHEWABLE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M009
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-836 \
  -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
71610-836-307161008363030 TABLET, CHEWABLE in 1 BOTTLE (71610-836-30)
71610-836-537161008365360 TABLET, CHEWABLE in 1 BOTTLE (71610-836-53)
71610-836-607161008366090 TABLET, CHEWABLE in 1 BOTTLE (71610-836-60)
71610-836-8071610083680180 TABLET, CHEWABLE in 1 BOTTLE (71610-836-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 71610-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-836. 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.