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PRAVASTATIN SODIUM

NDC 71610-879, PRAVASTATIN SODIUM, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-879
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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/71610-879 \
  -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
71610-879-457161008794545 TABLET in 1 BOTTLE (71610-879-45)
71610-879-537161008795360 TABLET in 1 BOTTLE (71610-879-53)
71610-879-607161008796090 TABLET in 1 BOTTLE (71610-879-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2e5cfae8-20b8-1fea-e063-6394a90a4e17

Use it

Look up 71610-879 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-879 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-879. 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.