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Losartan Potassium

NDC 42708-055, Losartan Potassium, tablet, film coated, from QPharma, Inc..

Product NDC
42708-055
Status
Listed
Labeler
QPharma, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090083
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-055 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOSARTAN POTASSIUM50 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]

Package NDCNDC-11Package
42708-055-304270800553030 TABLET, FILM COATED in 1 BOTTLE (42708-055-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2a7513c4-b73b-46fe-ba86-6e58658cdbc7

Use it

Look up 42708-055 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-055 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-055. 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.