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FOSAMAX

NDC 78206-135, alendronate sodium, tablet, from Organon LLC.

Product NDC
78206-135
Status
Listed
Labeler
Organon LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020560
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/78206-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALENDRONATE SODIUM70 mg/1

Pharmacologic classes

Bisphosphonate [EPC]; Diphosphonates [CS]

Package NDCNDC-11Package
78206-135-01782060135014 TABLET in 1 BLISTER PACK (78206-135-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/14e931fd-2c5f-4d90-b7db-5980706f4a56
  • NADAC price for package 78206013501

    GET /v1/drugs/nadac/78206013501

Use it

Look up 78206-135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/78206-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 78206-135. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.