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PRAVASTATIN SODIUM

NDC 71205-149, PRAVASTATIN SODIUM, tablet, from Proficient Rx LP.

Product NDC
71205-149
Status
Listed
Labeler
Proficient Rx LP
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/71205-149 \
  -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
71205-149-307120501493030 TABLET in 1 BOTTLE (71205-149-30)
71205-149-607120501496060 TABLET in 1 BOTTLE (71205-149-60)
71205-149-907120501499090 TABLET in 1 BOTTLE (71205-149-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d2b4607-0a46-4b58-9247-dc448ce258ec

Use it

Look up 71205-149 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-149 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-149. 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.