Package 68382-092-17

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 68382-092-17
Digits Only 6838209217
Product NDC 68382-092
Product ID 68382-092_a7e5dd69-ac10-4f36-a366-4ddc1426aef1
Description

28 TABLET, FILM COATED in 1 BOTTLE (68382-092-17)

Marketing

Marketing Status
Marketed Since 2007-09-05
Brand carvedilol
Generic carvedilol
Sample Package No

Linked Drug Pages (1)

Carvedilol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a7e5dd69-ac10-4f36-a366-4ddc1426aef1", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200032", "200033", "686924"], "spl_set_id": ["dc6a2d33-aa04-4a04-9cde-901b744d24ca"], "pharm_class_epc": ["alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-092-01)", "package_ndc": "68382-092-01", "marketing_start_date": "20070905"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-092-05)", "package_ndc": "68382-092-05", "marketing_start_date": "20070905"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68382-092-17)", "package_ndc": "68382-092-17", "marketing_start_date": "20070905"}], "brand_name": "Carvedilol", "product_id": "68382-092_a7e5dd69-ac10-4f36-a366-4ddc1426aef1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68382-092", "generic_name": "Carvedilol", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "3.125 mg/1"}], "application_number": "ANDA077614", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20271231"}