Package 65862-237-03

Brand: ibandronate sodium

Generic: ibandronate sodium
NDC Package

Package Facts

Identity

Package NDC 65862-237-03
Digits Only 6586223703
Product NDC 65862-237
Product ID 65862-237_6d9a3f36-83b1-4d1b-ab7d-582b3551839b
Description

1 BLISTER PACK in 1 CARTON (65862-237-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-03-11
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": "6d9a3f36-83b1-4d1b-ab7d-582b3551839b", "openfda": {"unii": ["J12U072QL0"], "rxcui": ["904932"], "spl_set_id": ["86c0b4ae-5e38-4efe-88af-50ac560e294f"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (65862-237-03)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-237-03", "marketing_start_date": "20160311"}], "brand_name": "Ibandronate Sodium", "product_id": "65862-237_6d9a3f36-83b1-4d1b-ab7d-582b3551839b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "65862-237", "generic_name": "Ibandronate Sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibandronate Sodium", "active_ingredients": [{"name": "IBANDRONATE SODIUM", "strength": "150 mg/1"}], "application_number": "ANDA204502", "marketing_category": "ANDA", "marketing_start_date": "20160311", "listing_expiration_date": "20271231"}