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PRAVASTATIN SODIUM

NDC 50090-7709, PRAVASTATIN SODIUM, tablet, from A-S Medication Solutions.

Product NDC
50090-7709
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7709 \
  -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
50090-7709-05009077090030 TABLET in 1 BOTTLE (50090-7709-0)
50090-7709-15009077090190 TABLET in 1 BOTTLE (50090-7709-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/635062df-9a84-4ff8-874c-dcee581a5555

Use it

Look up 50090-7709 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7709 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7709. 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.