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Pravastatin Sodium

NDC 71205-294, Pravastatin Sodium, tablet, from Proficient Rx LP.

Product NDC
71205-294
Status
Listed
Labeler
Proficient Rx LP
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/71205-294 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-294-307120502943030 TABLET in 1 BOTTLE (71205-294-30)
71205-294-607120502946060 TABLET in 1 BOTTLE (71205-294-60)
71205-294-907120502949090 TABLET in 1 BOTTLE (71205-294-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/466e2d1a-a6d6-40f8-a9f6-3e7494a34ca6

Use it

Look up 71205-294 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-294 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-294. 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.