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PRAVASTATIN SODIUM

NDC 68071-3361, PRAVASTATIN SODIUM, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-3361
Status
Listed
Labeler
NuCare 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/68071-3361 \
  -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
68071-3361-36807133610330 TABLET in 1 BOTTLE (68071-3361-3)
68071-3361-96807133610990 TABLET in 1 BOTTLE (68071-3361-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/54228087-7ab0-5561-e054-00144ff8d46c

Use it

Look up 68071-3361 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3361 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3361. 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.