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VALSARTAN AND HYDROCHLOROTHIAZIDE

NDC 50228-151, valsartan and hydrochlorothiazide, tablet, film coated, from ScieGen Pharmaceuticals, INC..

Product NDC
50228-151
Status
Listed
Labeler
ScieGen Pharmaceuticals, INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204687
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-151 \
  -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
50228-151-0550228015105500 TABLET, FILM COATED in 1 BOTTLE (50228-151-05)
50228-151-305022801513030 TABLET, FILM COATED in 1 BOTTLE (50228-151-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/17362ff8-07bb-42c6-a100-8adb93be0348

Use it

Look up 50228-151 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-151 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-151. 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.