Package 0093-3099-56

Brand: risedronate sodium

Generic: risedronate sodium
NDC Package

Package Facts

Identity

Package NDC 0093-3099-56
Digits Only 0093309956
Product NDC 0093-3099
Product ID 0093-3099_5495c43b-77b2-4ac7-b138-7cac84cca3ba
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-3099-56)

Marketing

Marketing Status
Marketed Since 2015-06-01
Brand risedronate sodium
Generic risedronate sodium
Sample Package No

Linked Drug Pages (1)

Risedronate Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5495c43b-77b2-4ac7-b138-7cac84cca3ba", "openfda": {"unii": ["F67L43UT5C"], "rxcui": ["905024", "905032", "905041", "905092", "905100"], "spl_set_id": ["dddcd321-4d2e-4643-bf3c-7b752b33ba39"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-3099-56)", "package_ndc": "0093-3099-56", "marketing_start_date": "20150601"}], "brand_name": "Risedronate Sodium", "product_id": "0093-3099_5495c43b-77b2-4ac7-b138-7cac84cca3ba", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "0093-3099", "generic_name": "Risedronate Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risedronate Sodium", "active_ingredients": [{"name": "RISEDRONATE SODIUM MONOHYDRATE", "strength": "5 mg/1"}], "application_number": "ANDA077132", "marketing_category": "ANDA", "marketing_start_date": "20150601", "listing_expiration_date": "20261231"}