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Losartan Potassium and Hydrochlorothiazide

NDC 70518-3398, losartan potassium and hydrochlorothiazide, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3398
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204901
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3398 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOSARTAN POTASSIUM100 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
70518-3398-17051833980190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3398-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fd07d24c-6db1-4f6b-b226-68abba3a3321

Use it

Look up 70518-3398 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3398 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3398. 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.