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PRAVASTATIN SODIUM

NDC 68788-7779, PRAVASTATIN SODIUM, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-7779
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076341
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7779 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68788-7779-36878877790390 TABLET in 1 BOTTLE (68788-7779-3)
68788-7779-668788777906100 TABLET in 1 BOTTLE (68788-7779-6)
68788-7779-968788777909500 TABLET in 1 BOTTLE (68788-7779-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6d42bd30-1f09-49f4-9ec8-31366df1b4b4

Use it

Look up 68788-7779 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7779 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7779. 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.