Package 50090-4171-4

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 50090-4171-4
Digits Only 5009041714
Product NDC 50090-4171
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-4171-4)

Marketing

Marketing Status
Marketed Since 2019-03-06
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": "fc284893-e0aa-4d94-bb4e-3d994e519613", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200033"], "spl_set_id": ["dd8b2a3f-c2fa-4859-84a1-c02f2b608748"], "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 (50090-4171-0)", "package_ndc": "50090-4171-0", "marketing_start_date": "20190306"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-4171-1)", "package_ndc": "50090-4171-1", "marketing_start_date": "20190306"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4171-3)", "package_ndc": "50090-4171-3", "marketing_start_date": "20210924"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4171-4)", "package_ndc": "50090-4171-4", "marketing_start_date": "20190306"}], "brand_name": "Carvedilol", "product_id": "50090-4171_fc284893-e0aa-4d94-bb4e-3d994e519613", "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": "50090-4171", "generic_name": "Carvedilol", "labeler_name": "A-S Medication Solutions", "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": "20070905", "listing_expiration_date": "20271231"}