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Pravastatin Sodium

NDC 69292-103, Pravastatin Sodium, tablet, from Amici Pharma, Inc..

Product NDC
69292-103
Status
Listed
Labeler
Amici Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077491
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69292-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM40 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Package NDCNDC-11Package
69292-103-10692920103101000 TABLET in 1 BOTTLE (69292-103-10)
69292-103-5069292010350500 TABLET in 1 BOTTLE (69292-103-50)
69292-103-906929201039090 TABLET in 1 BOTTLE (69292-103-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6551230-fe4c-4a6e-9c19-ae9945b76db0

Use it

Look up 69292-103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69292-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69292-103. 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.