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LOSARTAN POTASSIUM

NDC 72865-142, LOSARTAN POTASSIUM, tablet, film coated, from XLCare Pharmaceuticals, Inc..

Product NDC
72865-142
Status
Listed
Labeler
XLCare Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203835
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-142 \
  -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
72865-142-10728650142101000 TABLET, FILM COATED in 1 BOTTLE (72865-142-10)
72865-142-307286501423030 TABLET, FILM COATED in 1 BOTTLE (72865-142-30)
72865-142-907286501429090 TABLET, FILM COATED in 1 BOTTLE (72865-142-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/20421665-0401-4f6e-9e1d-232c654efb0f

Use it

Look up 72865-142 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-142 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-142. 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.