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PRAVASTATIN SODIUM

NDC 50268-667, PRAVASTATIN SODIUM, tablet, from AvPAK.

Product NDC
50268-667
Status
Listed
Labeler
AvPAK
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076341
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-667 \
  -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
50268-667-155026806671550 BLISTER PACK in 1 BOX (50268-667-15) / 1 TABLET in 1 BLISTER PACK (50268-667-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ba4ac602-46fa-8386-e053-2995a90a9764

  • NADAC price for package 50268066715

    GET /v1/drugs/nadac/50268066715

Use it

Look up 50268-667 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-667 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-667. 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.