Package 68788-9265-1

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 68788-9265-1
Digits Only 6878892651
Product NDC 68788-9265
Description

100 TABLET, FILM COATED in 1 BOTTLE (68788-9265-1)

Marketing

Marketing Status
Marketed Since 2014-12-03
Brand carvedilol
Generic carvedilol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8cbf4bb1-72f2-4e70-9a43-ba62d8fb3317", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200033"], "spl_set_id": ["81bc612d-5674-45b9-a1f5-2cb4fa625747"], "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": ["Preferred Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-9265-1)", "package_ndc": "68788-9265-1", "marketing_start_date": "20141203"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-9265-3)", "package_ndc": "68788-9265-3", "marketing_start_date": "20141203"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-9265-6)", "package_ndc": "68788-9265-6", "marketing_start_date": "20141203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-9265-9)", "package_ndc": "68788-9265-9", "marketing_start_date": "20141203"}], "brand_name": "Carvedilol", "product_id": "68788-9265_8cbf4bb1-72f2-4e70-9a43-ba62d8fb3317", "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": "68788-9265", "generic_name": "Carvedilol", "labeler_name": "Preferred Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "25 mg/1"}], "application_number": "ANDA077614", "marketing_category": "ANDA", "marketing_start_date": "20141203", "listing_expiration_date": "20261231"}