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Alendronate Sodium

NDC 65862-327, Alendronate Sodium, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-327
Status
Listed
Labeler
Aurobindo Pharma Limited
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/65862-327 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALENDRONATE SODIUM10 mg/1

Pharmacologic classes

Bisphosphonate [EPC]; Diphosphonates [CS]

Package NDCNDC-11Package
65862-327-0165862032701100 TABLET in 1 BOTTLE (65862-327-01)
65862-327-106586203271010 BLISTER PACK in 1 CARTON (65862-327-10) / 10 TABLET in 1 BLISTER PACK
65862-327-306586203273030 TABLET in 1 BOTTLE (65862-327-30)
65862-327-99658620327991000 TABLET in 1 BOTTLE (65862-327-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/815a87c4-e489-4eb9-9a2e-fb7a16642f01

Use it

Look up 65862-327 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-327 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-327. 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.