Package 65862-144-01

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 65862-144-01
Digits Only 6586214401
Product NDC 65862-144
Product ID 65862-144_f210723f-29fb-46c7-8ac4-5009d9696d3b
Description

100 TABLET, FILM COATED in 1 BOTTLE (65862-144-01)

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": "f210723f-29fb-46c7-8ac4-5009d9696d3b", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200032", "200033", "686924"], "spl_set_id": ["7cc14b86-0833-4c3c-91f3-7963d7052fd5"], "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": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-144-01)", "package_ndc": "65862-144-01", "marketing_start_date": "20070905"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-144-05)", "package_ndc": "65862-144-05", "marketing_start_date": "20070905"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-144-99)", "package_ndc": "65862-144-99", "marketing_start_date": "20070905"}], "brand_name": "Carvedilol", "product_id": "65862-144_f210723f-29fb-46c7-8ac4-5009d9696d3b", "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": "65862-144", "generic_name": "Carvedilol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "12.5 mg/1"}], "application_number": "ANDA078332", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}