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Valsartan

NDC 29300-235, Valsartan, tablet, film coated, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-235
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209261
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALSARTAN320 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]

Package NDCNDC-11Package
29300-235-10293000235101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-10)
29300-235-132930002351330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-13)
29300-235-192930002351990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-19)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/93b82a9f-dc0a-4f7d-b0d4-4adf0d917b7e

Use it

Look up 29300-235 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-235. 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.