Package 50090-1062-2

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 50090-1062-2
Digits Only 5009010622
Product NDC 50090-1062
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-1062-2)

Marketing

Marketing Status
Marketed Since 2014-11-28
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": "ae7a30de-d871-4967-a26d-db3b329a7fa8", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["686924"], "spl_set_id": ["3eb4fd8e-1027-4d24-8f2f-12e9dcfe6231"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-1062-0)", "package_ndc": "50090-1062-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-1062-1)", "package_ndc": "50090-1062-1", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-1062-2)", "package_ndc": "50090-1062-2", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-1062-3)", "package_ndc": "50090-1062-3", "marketing_start_date": "20231128"}], "brand_name": "Carvedilol", "product_id": "50090-1062_ae7a30de-d871-4967-a26d-db3b329a7fa8", "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": "50090-1062", "generic_name": "Carvedilol", "labeler_name": "A-S Medication Solutions", "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"}