Package 42708-072-60

Brand: carvedilol

Generic: carvedilol
NDC Package Sample

Package Facts

Identity

Package NDC 42708-072-60
Digits Only 4270807260
Product NDC 42708-072
Description

60 TABLET, FILM COATED in 1 BOTTLE (42708-072-60)

Marketing

Marketing Status
Marketed Since 2018-04-18
Brand carvedilol
Generic carvedilol
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b3b81e-d875-5d61-e063-6394a90ad20a", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["686924"], "spl_set_id": ["ffbedcce-0d64-4aed-9e65-09448d71ca91"], "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": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "60 TABLET, FILM COATED in 1 BOTTLE (42708-072-60)", "package_ndc": "42708-072-60", "marketing_start_date": "20180418"}], "brand_name": "Carvedilol", "product_id": "42708-072_45b3b81e-d875-5d61-e063-6394a90ad20a", "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": "42708-072", "generic_name": "Carvedilol", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "3.125 mg/1"}], "application_number": "ANDA076373", "marketing_category": "ANDA", "marketing_start_date": "20070906", "listing_expiration_date": "20261231"}