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VALSARTAN

NDC 51660-142, VALSARTAN, tablet, film coated, from Ohm Laboratories Inc..

Product NDC
51660-142
Status
Listed
Labeler
Ohm Laboratories Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077492
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51660-142 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALSARTAN160 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51660-142-035166001420310 TABLET, FILM COATED in 1 BOTTLE (51660-142-03)
51660-142-0551660014205500 TABLET, FILM COATED in 1 BOTTLE (51660-142-05)
51660-142-905166001429090 TABLET, FILM COATED in 1 BOTTLE (51660-142-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ab5e0e5a-5bdf-4cfc-9d18-57ea4d642f65

  • NADAC price for package 51660014290

    GET /v1/drugs/nadac/51660014290

Use it

Look up 51660-142 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51660-142 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51660-142. 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.