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losartan potassium and hydrochlorothiazide

NDC 71335-2662, losartan potassium and hydrochlorothiazide, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2662
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204832
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2662 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE12.5 mg/1
  • LOSARTAN POTASSIUM100 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
71335-2662-17133526620130 TABLET, FILM COATED in 1 BOTTLE (71335-2662-1)
71335-2662-27133526620290 TABLET, FILM COATED in 1 BOTTLE (71335-2662-2)
71335-2662-371335266203120 TABLET, FILM COATED in 1 BOTTLE (71335-2662-3)
71335-2662-471335266204100 TABLET, FILM COATED in 1 BOTTLE (71335-2662-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eb423f4b-8104-4406-bfc2-8943e517329f

Use it

Look up 71335-2662 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2662 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.