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PRAVASTATIN SODIUM

NDC 71610-884, PRAVASTATIN SODIUM, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-884
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209869
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-884 \
  -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
71610-884-457161008844545 TABLET in 1 BOTTLE (71610-884-45)
71610-884-537161008845360 TABLET in 1 BOTTLE (71610-884-53)
71610-884-607161008846090 TABLET in 1 BOTTLE (71610-884-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/308db0cc-0deb-99b6-e063-6394a90a9b74

Use it

Look up 71610-884 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-884 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-884. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.