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Alendronate Sodium

NDC 71205-048, Alendronate Sodium, tablet, from Proficient Rx LP.

Product NDC
71205-048
Status
Listed
Labeler
Proficient Rx LP
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/71205-048 \
  -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
71205-048-04712050048041 BLISTER PACK in 1 CARTON (71205-048-04) / 4 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6c4d13fb-490c-4ea9-9b04-003c8d8e9f0c

Use it

Look up 71205-048 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-048 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-048. 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.