Package 64980-342-50
Brand: alendronate sodium
Generic: alendronate sodiumPackage Facts
Identity
Package NDC
64980-342-50
Digits Only
6498034250
Product NDC
64980-342
Description
500 TABLET in 1 BOTTLE (64980-342-50)
Marketing
Marketing Status
Brand
alendronate sodium
Generic
alendronate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f943241-8c1a-4261-a337-f2fc45ad2835", "openfda": {"upc": ["0364980340038", "0364980342148", "0364980342018", "0364980340014"], "unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904419", "904431"], "spl_set_id": ["ffdd2496-d253-419b-85a6-8c615f7545f1"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-342-01)", "package_ndc": "64980-342-01", "marketing_start_date": "20240930"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (64980-342-14) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "64980-342-14", "marketing_start_date": "20080804"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64980-342-50)", "package_ndc": "64980-342-50", "marketing_start_date": "20240930"}], "brand_name": "Alendronate Sodium", "product_id": "64980-342_3f943241-8c1a-4261-a337-f2fc45ad2835", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "64980-342", "generic_name": "Alendronate Sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "ANDA090124", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}