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Pravastatin Sodium

NDC 0480-7270, Pravastatin Sodium, tablet, from Teva Pharmaceuticals, Inc..

Product NDC
0480-7270
Status
Listed
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077793
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0480-7270 \
  -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
0480-7270-10004807270101000 TABLET in 1 BOTTLE (0480-7270-10)
0480-7270-980048072709890 TABLET in 1 BOTTLE (0480-7270-98)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f66cb1c1-5ff1-4b0b-89d0-8ecaee26b0b8

Use it

Look up 0480-7270 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0480-7270 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0480-7270. 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.