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Alendronate Sodium

NDC 0115-1679, Alendronate Sodium, tablet, from Amneal Pharmaceuticals of New York LLC.

Product NDC
0115-1679
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075710
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0115-1679 \
  -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
0115-1679-260011516792612 BLISTER PACK in 1 CARTON (0115-1679-26) / 1 TABLET in 1 BLISTER PACK (0115-1679-30)
0115-1679-34001151679344 BLISTER PACK in 1 CARTON (0115-1679-34) / 1 TABLET in 1 BLISTER PACK (0115-1679-30)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c23fb7fe-c6b9-4f77-bde7-992222b589d3

Use it

Look up 0115-1679 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0115-1679 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0115-1679. 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.