Package 65862-870-03

Brand: risedronate sodium

Generic: risedronate sodium
NDC Package

Package Facts

Identity

Package NDC 65862-870-03
Digits Only 6586287003
Product NDC 65862-870
Description

1 BLISTER PACK in 1 CARTON (65862-870-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-10-21
Brand risedronate sodium
Generic risedronate sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bb13e9ba-84fc-41b6-b2f9-bedd9f3eef1f", "openfda": {"unii": ["OFG5EXG60L"], "rxcui": ["905028"], "spl_set_id": ["a42a35e6-3e08-4b4f-ae56-47d4aec2322a"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (65862-870-03)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-870-03", "marketing_start_date": "20161021"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (65862-870-11)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-870-11", "marketing_start_date": "20161021"}], "brand_name": "Risedronate Sodium", "product_id": "65862-870_bb13e9ba-84fc-41b6-b2f9-bedd9f3eef1f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "65862-870", "generic_name": "Risedronate Sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risedronate Sodium", "active_ingredients": [{"name": "RISEDRONATE SODIUM", "strength": "150 mg/1"}], "application_number": "ANDA206768", "marketing_category": "ANDA", "marketing_start_date": "20161021", "listing_expiration_date": "20271231"}