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PRAVASTATIN SODIUM

NDC 71610-877, PRAVASTATIN SODIUM, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-877
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/71610-877 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71610-877-307161008773030 TABLET in 1 BOTTLE (71610-877-30)
71610-877-457161008774545 TABLET in 1 BOTTLE (71610-877-45)
71610-877-537161008775360 TABLET in 1 BOTTLE (71610-877-53)
71610-877-607161008776090 TABLET in 1 BOTTLE (71610-877-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2e5c8a1c-b36f-d124-e063-6394a90a6fb5

Use it

Look up 71610-877 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-877 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-877. 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.