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Pravastatin Sodium

NDC 16714-559, Pravastatin Sodium, tablet, from NorthStar RxLLC.

Product NDC
16714-559
Status
Listed
Labeler
NorthStar RxLLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-559 \
  -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
16714-559-011671405590190 TABLET in 1 BOTTLE (16714-559-01)
16714-559-0216714055902500 TABLET in 1 BOTTLE (16714-559-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce15ad07-3286-478f-9f30-1db6a45ed402

  • NADAC price for package 16714055901

    GET /v1/drugs/nadac/16714055901

  • NADAC price for package 16714055902

    GET /v1/drugs/nadac/16714055902

Use it

Look up 16714-559 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-559 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-559. 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.