Package 60723-205-31
Brand: alendronate
Generic: alendronate sodiumPackage Facts
Identity
Package NDC
60723-205-31
Digits Only
6072320531
Product NDC
60723-205
Description
1 BLISTER PACK in 1 CARTON (60723-205-31) / 4 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
alendronate
Generic
alendronate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "460d461d-4807-2ed0-e063-6394a90aad4a", "openfda": {"upc": ["0360723207330"], "unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904431"], "spl_set_id": ["a24fd39c-34a7-4de2-9439-781e612189ca"], "manufacturer_name": ["Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (60723-205-31) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "60723-205-31", "marketing_start_date": "20171205"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (60723-205-32) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "60723-205-32", "marketing_start_date": "20171205"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (60723-205-33) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "60723-205-33", "marketing_start_date": "20171205"}], "brand_name": "Alendronate", "product_id": "60723-205_460d461d-4807-2ed0-e063-6394a90aad4a", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "60723-205", "generic_name": "ALENDRONATE SODIUM", "labeler_name": "Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "ANDA090258", "marketing_category": "ANDA", "marketing_start_date": "20171205", "listing_expiration_date": "20261231"}