Package 60505-2795-0
Brand: ibandronate sodium
Generic: ibandronate sodiumPackage Facts
Identity
Package NDC
60505-2795-0
Digits Only
6050527950
Product NDC
60505-2795
Description
3 BLISTER PACK in 1 PACKAGE (60505-2795-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
ibandronate sodium
Generic
ibandronate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31cdb988-ed22-4f0d-d1c2-8e89aae8c703", "openfda": {"unii": ["J12U072QL0"], "rxcui": ["904932"], "spl_set_id": ["dd674424-b151-d7eb-3acf-b1589347f2f7"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 PACKAGE (60505-2795-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "60505-2795-0", "marketing_start_date": "20120319"}], "brand_name": "IBANDRONATE SODIUM", "product_id": "60505-2795_31cdb988-ed22-4f0d-d1c2-8e89aae8c703", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "60505-2795", "generic_name": "IBANDRONATE SODIUM", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBANDRONATE SODIUM", "active_ingredients": [{"name": "IBANDRONATE SODIUM", "strength": "150 mg/1"}], "application_number": "ANDA078948", "marketing_category": "ANDA", "marketing_start_date": "20120319", "listing_expiration_date": "20271231"}