Alendronate Sodium

Orange BookUNIISPLATC M05BA04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAurobindo Pharma Limited

CountryUS (United States)

ATC codeM05BA04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
6586232804
1 BLISTER PACK in 1 CARTON (65862-328-04) / 4 TABLET in 1 BLISTER PACK
ndc11
6586232808
3 BLISTER PACK in 1 CARTON (65862-328-08) / 4 TABLET in 1 BLISTER PACK
ndc11
6586232810
10 BLISTER PACK in 1 CARTON (65862-328-10) / 10 TABLET in 1 BLISTER PACK
ndc11
6586232820
5 BLISTER PACK in 1 CARTON (65862-328-20) / 4 TABLET in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)

2UY4M2U3RA

ALENDRONATE SODIUM

RxCUI 203152

Orange Book

A090124

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "2UY4M2U3RA",
    "rxcui": "203152",
    "inchikey": "DCSBSVSZJRSITC-UHFFFAOYSA-M",
    "display_name": "ALENDRONATE SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "815a87c4-e489-4eb9-9a2e-fb7a16642f01": {
      "match": "brand_token",
      "title": "ALENDRONATE SODIUM TABLET [AUROBINDO PHARMA LIMITED]",
      "spl_version": "27",
      "published_date": "2026-05-26"
    }
  },
  "productid": "65862-328_c2dfac3c-41f9-42fa-bb6b-54b3fd9d1512",
  "productndc": "65862-328",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "090124",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Aug 4, 2008"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 35MG BASE",
        "product_no": "002",
        "approval_date": "Aug 4, 2008"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 70MG BASE",
        "product_no": "003",
        "approval_date": "Aug 4, 2008"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ALENDRONATE SODIUM",
  "proprietary_name": "Alendronate Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090124",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Alendronate Sodium",
  "start_marketing_date": "20080804",
  "active_numerator_strength": "35"
}

Related drugs

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