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Losartan Potassium

NDC 71610-207, Losartan potassium, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-207
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091497
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-207 \
  -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
71610-207-307161002073030 TABLET, FILM COATED in 1 BOTTLE (71610-207-30)
71610-207-457161002074545 TABLET, FILM COATED in 1 BOTTLE (71610-207-45)
71610-207-607161002076090 TABLET, FILM COATED in 1 BOTTLE (71610-207-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f55aaa2-5848-47e0-bba0-6a70b2fa05dd

Use it

Look up 71610-207 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-207 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-207. 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.