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Valsartan and Hydrochlorothiazide

NDC 53746-849, Valsartan and Hydrochlorothiazide, tablet, film coated, from Amneal Pharmaceuticals of New York LLC.

Product NDC
53746-849
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204382
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/53746-849 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALSARTAN320 mg/1
  • HYDROCHLOROTHIAZIDE25 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
53746-849-905374608499090 TABLET, FILM COATED in 1 BOTTLE (53746-849-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5a1db33-3046-407c-a557-6b41642164a9

Use it

Look up 53746-849 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53746-849 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53746-849. 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.