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sacubitril and valsartan

NDC 70771-1922, sacubitril and valsartan, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1922
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213719
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1922 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SACUBITRIL49 mg/1
  • VALSARTAN51 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1922-47077119220410 BLISTER PACK in 1 CARTON (70771-1922-4) / 10 TABLET in 1 BLISTER PACK (70771-1922-2)
70771-1922-67077119220660 TABLET in 1 BOTTLE (70771-1922-6)
70771-1922-870771192208180 TABLET in 1 BOTTLE (70771-1922-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4c871c01-0564-411f-87e2-478aa42503cf

Use it

Look up 70771-1922 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1922 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1922. 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.