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PRAVASTATIN SODIUM

NDC 68180-485, PRAVASTATIN SODIUM, tablet, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-485
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077917
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68180-485 \
  -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

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1123d56c-16f0-4f81-b56f-67b1f343ae1e

Use it

Look up 68180-485 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-485 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-485. 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.