Package 47335-928-67

Brand: risedronate sodium

Generic: risedronate sodium
NDC Package

Package Facts

Identity

Package NDC 47335-928-67
Digits Only 4733592867
Product NDC 47335-928
Description

3 BLISTER PACK in 1 CARTON (47335-928-67) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-06-11
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": "a9910c38-e099-4f8a-a7e9-a88623be2032", "openfda": {"upc": ["0347335727982"], "unii": ["HU2YAQ274O"], "rxcui": ["905024", "905028", "905032", "905041", "905083", "905092", "905100"], "spl_set_id": ["e0b5f0ed-ff40-4f0d-bb86-81a7ace9f339"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (47335-928-60)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "47335-928-60", "marketing_start_date": "20140611"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (47335-928-67)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "47335-928-67", "marketing_start_date": "20140611"}], "brand_name": "risedronate sodium", "product_id": "47335-928_a9910c38-e099-4f8a-a7e9-a88623be2032", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "47335-928", "generic_name": "risedronate sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "risedronate sodium", "active_ingredients": [{"name": "RISEDRONATE SODIUM HEMI-PENTAHYDRATE", "strength": "150 mg/1"}], "application_number": "ANDA090886", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20271231"}