🇺🇸
United States · US · US:68788-7130_e88fb31d-cfc6-4e20-95fa-90fa26bf8644
ALENDRONATE SODIUM
Orange BookUNIISPLATC M05BA04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPreferred Pharmaceuticals Inc.
CountryUS (United States)
ATC codeM05BA04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1168788713044 TABLET in 1 BLISTER PACK (68788-7130-4)
Annotations
UNII (FDA Substance ID)
2UY4M2U3RA
ALENDRONATE SODIUM
RxCUI 203152
Orange Book
A076768
ABABABABAB
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": "68788-7130_e88fb31d-cfc6-4e20-95fa-90fa26bf8644",
"productndc": "68788-7130",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "076768",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 5MG BASE",
"product_no": "001",
"approval_date": "Aug 4, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 10MG BASE",
"product_no": "002",
"approval_date": "Aug 4, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 35MG BASE",
"product_no": "003",
"approval_date": "Aug 4, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 40MG BASE",
"product_no": "004",
"approval_date": "Aug 4, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 70MG BASE",
"product_no": "005",
"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": "ANDA076768",
"marketing_category": "ANDA",
"nonproprietary_name": "Alendronate sodium",
"start_marketing_date": "20180330",
"active_numerator_strength": "70"
}Related drugs
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