Package 71205-714-04

Brand: risedronate sodium

Generic: risedronate sodium
NDC Package

Package Facts

Identity

Package NDC 71205-714-04
Digits Only 7120571404
Product NDC 71205-714
Description

1 BLISTER PACK in 1 CARTON (71205-714-04) / 4 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-11-10
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": "81702f21-3117-49ce-8e9b-2aa2648ba7c3", "openfda": {"upc": ["0371205714048"], "unii": ["OFG5EXG60L"], "rxcui": ["905024"], "spl_set_id": ["81702f21-3117-49ce-8e9b-2aa2648ba7c3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-714-04)  / 4 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-714-04", "marketing_start_date": "20221110"}], "brand_name": "Risedronate Sodium", "product_id": "71205-714_81702f21-3117-49ce-8e9b-2aa2648ba7c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "71205-714", "generic_name": "Risedronate Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risedronate Sodium", "active_ingredients": [{"name": "RISEDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA090877", "marketing_category": "ANDA", "marketing_start_date": "20151130", "listing_expiration_date": "20261231"}