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Pravastatin sodium

NDC 70377-048, Pravastatin sodium, tablet, from Biocon Pharma Inc..

Product NDC
70377-048
Status
Listed
Labeler
Biocon Pharma Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209869
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70377-048 \
  -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
70377-048-117037700481130 TABLET in 1 BOTTLE (70377-048-11)
70377-048-127037700481290 TABLET in 1 BOTTLE (70377-048-12)
70377-048-1370377004813500 TABLET in 1 BOTTLE (70377-048-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9bd4a493-1f75-e33a-53fb-4e2fbc64a1eb

  • NADAC price for package 70377004812

    GET /v1/drugs/nadac/70377004812

  • NADAC price for package 70377004813

    GET /v1/drugs/nadac/70377004813

Use it

Look up 70377-048 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70377-048 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70377-048. 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.