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Sacubitril and Valsartan

NDC 60290-087, Sacubitril and Valsartan, tablet, film coated, from Umedica Laboratories USA Inc..

Product NDC
60290-087
Status
Listed
Labeler
Umedica Laboratories USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219946
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60290-087 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SACUBITRIL97 mg/1
  • VALSARTAN103 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Neprilysin Inhibitor [EPC]; Neprilysin Inhibitors [MoA]

Package NDCNDC-11Package
60290-087-016029000870160 TABLET, FILM COATED in 1 BOTTLE (60290-087-01)
60290-087-0260290008702180 TABLET, FILM COATED in 1 BOTTLE (60290-087-02)
60290-087-03602900087031000 TABLET, FILM COATED in 1 BOTTLE (60290-087-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3173e592-6f28-4864-9bf0-0ef0452da3de

Use it

Look up 60290-087 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60290-087 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60290-087. 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.