Package 50090-2322-1
Brand: alendronate sodium
Generic: alendronate sodiumPackage Facts
Identity
Package NDC
50090-2322-1
Digits Only
5009023221
Product NDC
50090-2322
Description
1 BLISTER PACK in 1 CARTON (50090-2322-1) / 12 TABLET in 1 BLISTER PACK
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": "386b9902-f04a-4d44-b5f8-3924ddb4a738", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["70c27a96-70b1-4d2a-959b-89361fd20c37"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-2322-0) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "50090-2322-0", "marketing_start_date": "20160302"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-2322-1) / 12 TABLET in 1 BLISTER PACK", "package_ndc": "50090-2322-1", "marketing_start_date": "20160302"}], "brand_name": "Alendronate Sodium", "product_id": "50090-2322_386b9902-f04a-4d44-b5f8-3924ddb4a738", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "50090-2322", "generic_name": "Alendronate Sodium", "labeler_name": "A-S Medication Solutions", "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"}