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Losartan Potassium

NDC 63187-830, Losartan potassium, tablet, film coated, from Proficient Rx LP.

Product NDC
63187-830
Status
Listed
Labeler
Proficient Rx LP
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/63187-830 \
  -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
63187-830-306318708303030 TABLET, FILM COATED in 1 BOTTLE (63187-830-30)
63187-830-606318708306060 TABLET, FILM COATED in 1 BOTTLE (63187-830-60)
63187-830-906318708309090 TABLET, FILM COATED in 1 BOTTLE (63187-830-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c0319153-3e35-4a84-aa63-935b1e0047d8

Use it

Look up 63187-830 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63187-830 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63187-830. 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.