Package 33342-150-53

Brand: ibandronate sodium

Generic: ibandronate sodium
NDC Package

Package Facts

Identity

Package NDC 33342-150-53
Digits Only 3334215053
Product NDC 33342-150
Product ID 33342-150_29367df4-fac5-4117-963c-3e40ed998461
Description

3 CARTON in 1 BOX (33342-150-53) / 1 BLISTER PACK in 1 CARTON (33342-150-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-12-31
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": "29367df4-fac5-4117-963c-3e40ed998461", "openfda": {"unii": ["J12U072QL0"], "rxcui": ["904932"], "spl_set_id": ["a5741ef6-0599-4657-8cda-2902ded4f680"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (33342-150-52)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-150-52", "marketing_start_date": "20250701"}, {"sample": false, "description": "3 CARTON in 1 BOX (33342-150-53)  / 1 BLISTER PACK in 1 CARTON (33342-150-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-150-53", "marketing_end_date": "20271231", "marketing_start_date": "20180613"}], "brand_name": "IBANDRONATE SODIUM", "product_id": "33342-150_29367df4-fac5-4117-963c-3e40ed998461", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "33342-150", "generic_name": "IBANDRONATE SODIUM", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBANDRONATE SODIUM", "active_ingredients": [{"name": "IBANDRONATE SODIUM", "strength": "150 mg/1"}], "application_number": "ANDA206887", "marketing_category": "ANDA", "marketing_start_date": "20180613", "listing_expiration_date": "20271231"}