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ALENDRONATE SODIUM

NDC 70518-1192, Alendronate sodium, tablet, from REMEDYREPACK INC..

Product NDC
70518-1192
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076768
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1192 \
  -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
70518-1192-1705181192013 BLISTER PACK in 1 CARTON (70518-1192-1) / 4 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c7e470d6-508e-466e-a78d-060bbbc9745c

Use it

Look up 70518-1192 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1192 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1192. 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.