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Alendronate

NDC 60723-207, ALENDRONATE SODIUM, tablet, from Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd..

Product NDC
60723-207
Status
Listed
Labeler
Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090258
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60723-207 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALENDRONATE SODIUM35 mg/1

Pharmacologic classes

Bisphosphonate [EPC]; Diphosphonates [CS]

Package NDCNDC-11Package
60723-207-31607230207311 BLISTER PACK in 1 CARTON (60723-207-31) / 4 TABLET in 1 BLISTER PACK
60723-207-32607230207323 BLISTER PACK in 1 CARTON (60723-207-32) / 4 TABLET in 1 BLISTER PACK
60723-207-33607230207332 BLISTER PACK in 1 CARTON (60723-207-33) / 10 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a24fd39c-34a7-4de2-9439-781e612189ca

Use it

Look up 60723-207 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60723-207 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60723-207. 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.