Package 69452-378-74

Brand: ibandronate sodium

Generic: ibandronate sodium
NDC Package

Package Facts

Identity

Package NDC 69452-378-74
Digits Only 6945237874
Product NDC 69452-378
Product ID 69452-378_7c860070-7f7a-4217-9cfb-f5536fd736b4
Description

1 BLISTER PACK in 1 CARTON (69452-378-74) / 3 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-05-26
Brand ibandronate sodium
Generic ibandronate sodium
Sample Package No

Linked Drug Pages (1)

IBANDRONATE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7c860070-7f7a-4217-9cfb-f5536fd736b4", "openfda": {"unii": ["J12U072QL0"], "rxcui": ["904932"], "spl_set_id": ["6ca94cce-a2bb-421f-bd8f-6b14bc2bd985"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69452-378-74)  / 3 TABLET in 1 BLISTER PACK", "package_ndc": "69452-378-74", "marketing_start_date": "20230526"}], "brand_name": "IBANDRONATE SODIUM", "product_id": "69452-378_7c860070-7f7a-4217-9cfb-f5536fd736b4", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "69452-378", "generic_name": "IBANDRONATE SODIUM", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBANDRONATE SODIUM", "active_ingredients": [{"name": "IBANDRONATE SODIUM", "strength": "150 mg/1"}], "application_number": "ANDA078998", "marketing_category": "ANDA", "marketing_start_date": "20230526", "listing_expiration_date": "20261231"}