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PRAVASTATIN SODIUM

NDC 60687-886, PRAVASTATIN SODIUM, tablet, from American Health Packaging.

Product NDC
60687-886
Status
Listed
Labeler
American Health Packaging
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/60687-886 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
60687-886-0160687088601100 BLISTER PACK in 1 CARTON (60687-886-01) / 1 TABLET in 1 BLISTER PACK (60687-886-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/97f826f0-b5c5-410c-b1f0-523873981e8d

  • NADAC price for package 60687088601

    GET /v1/drugs/nadac/60687088601

Use it

Look up 60687-886 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-886 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-886. 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.