Package 68462-163-01

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 68462-163-01
Digits Only 6846216301
Product NDC 68462-163
Description

100 TABLET, FILM COATED in 1 BOTTLE (68462-163-01)

Marketing

Marketing Status
Marketed Since 2007-09-05
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": "5f5b2d20-cc2a-4e91-b2b9-260e7438ab2c", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "upc": ["0368462162019", "0368462163016", "0368462164013", "0368462165010"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200032", "200033", "686924"], "spl_set_id": ["c4a21f67-7812-4634-beba-f8e85c63c5f2"], "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": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-163-01)", "package_ndc": "68462-163-01", "marketing_start_date": "20070905"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68462-163-05)", "package_ndc": "68462-163-05", "marketing_start_date": "20070905"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68462-163-10)", "package_ndc": "68462-163-10", "marketing_start_date": "20070905"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68462-163-18)", "package_ndc": "68462-163-18", "marketing_start_date": "20141210"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68462-163-60)", "package_ndc": "68462-163-60", "marketing_start_date": "20070905"}], "brand_name": "Carvedilol", "product_id": "68462-163_5f5b2d20-cc2a-4e91-b2b9-260e7438ab2c", "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": "68462-163", "generic_name": "Carvedilol", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "6.25 mg/1"}], "application_number": "ANDA078251", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}