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Alendronate Sodium

NDC 16714-631, Alendronate Sodium, tablet, from NorthStar Rx LLC.

Product NDC
16714-631
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090124
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-631 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALENDRONATE SODIUM10 mg/1

Pharmacologic classes

Bisphosphonate [EPC]; Diphosphonates [CS]

Package NDCNDC-11Package
16714-631-011671406310130 TABLET in 1 BOTTLE (16714-631-01)
16714-631-0216714063102100 TABLET in 1 BOTTLE (16714-631-02)
16714-631-111671406311110 BLISTER PACK in 1 CARTON (16714-631-11) / 10 TABLET in 1 BLISTER PACK (16714-631-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4323d3aa-cbb0-41e2-aba7-7a94a0516993

  • NADAC price for package 16714063101

    GET /v1/drugs/nadac/16714063101

  • NADAC price for package 16714063102

    GET /v1/drugs/nadac/16714063102

Use it

Look up 16714-631 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-631 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-631. 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.