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Pravastatin sodium

NDC 68788-4059, Pravastatin sodium, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4059
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076056
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4059 \
  -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
68788-4059-36878840590330 TABLET in 1 BOTTLE (68788-4059-3)
68788-4059-66878840590660 TABLET in 1 BOTTLE (68788-4059-6)
68788-4059-96878840590990 TABLET in 1 BOTTLE (68788-4059-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f92e12bc-40c3-4afa-9190-2f4de11ec6b3

Use it

Look up 68788-4059 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4059 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4059. 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.