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Pravastatin sodium

NDC 65862-633, Pravastatin sodium, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-633
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203367
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-633 \
  -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
65862-633-0565862063305500 TABLET in 1 BOTTLE (65862-633-05)
65862-633-906586206339090 TABLET in 1 BOTTLE (65862-633-90)
65862-633-99658620633991000 TABLET in 1 BOTTLE (65862-633-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b06ed801-ddee-4f56-924a-59fcb451eae6

Use it

Look up 65862-633 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-633 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-633. 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.