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United States · US · US:64980-340_ac73eca3-eeb7-4be7-9b03-471c4941e5e7
Alendronate Sodium
Orange BookUNIISPLATC M05BA04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeM05BA04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116498034001100 TABLET in 1 BOTTLE (64980-340-01)
- ndc11649803400330 TABLET in 1 BOTTLE (64980-340-03)
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": "64980-340_ac73eca3-eeb7-4be7-9b03-471c4941e5e7",
"productndc": "64980-340",
"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": "10"
}Related drugs
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