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PRAVASTATIN SODIUM

NDC 0904-5892, PRAVASTATIN SODIUM, tablet, from Major Pharmaceuticals.

Product NDC
0904-5892
Status
Listed
Labeler
Major Pharmaceuticals
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/0904-5892 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0904-5892-6100904589261100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5892-61) / 1 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1d5bce9c-a788-4c52-a69e-c53174b8d061

  • NADAC price for package 00904589261

    GET /v1/drugs/nadac/00904589261

Use it

Look up 0904-5892 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-5892 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-5892. 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.