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Mefloquine Hydrochloride

NDC 0555-0171, Mefloquine Hydrochloride, tablet, from Teva Pharmaceuticals USA, Inc..

Product NDC
0555-0171
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076392
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0555-0171 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEFLOQUINE HYDROCHLORIDE250 mg/1

Pharmacologic classes

Antimalarial [EPC]

Package NDCNDC-11Package
0555-0171-780055501717825 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/09716a24-d7da-42b2-af29-c03a1b6670bd

  • NADAC price for package 00555017178

    GET /v1/drugs/nadac/00555017178

Use it

Look up 0555-0171 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0555-0171 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0555-0171. 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.