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Pravastatin Sodium

NDC 68462-198, Pravastatin Sodium, tablet, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-198
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
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/68462-198 \
  -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
68462-198-0568462019805500 TABLET in 1 BOTTLE (68462-198-05)
68462-198-906846201989090 TABLET in 1 BOTTLE (68462-198-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6ca01de3-a0f9-4cfb-b36a-723c7c42e2a4

  • NADAC price for package 68462019890

    GET /v1/drugs/nadac/68462019890

Use it

Look up 68462-198 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-198 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-198. 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.