Package 68788-7539-1

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 68788-7539-1
Digits Only 6878875391
Product NDC 68788-7539
Description

100 TABLET, FILM COATED in 1 BOTTLE (68788-7539-1)

Marketing

Marketing Status
Marketed Since 2019-12-27
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": "ec264427-b2b2-4da7-94d6-18fdd7eaffd7", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200032"], "spl_set_id": ["5c34847d-68f9-4967-81c8-a2297a6acb7f"], "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": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7539-1)", "package_ndc": "68788-7539-1", "marketing_start_date": "20191227"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7539-3)", "package_ndc": "68788-7539-3", "marketing_start_date": "20191227"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7539-6)", "package_ndc": "68788-7539-6", "marketing_start_date": "20191227"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7539-9)", "package_ndc": "68788-7539-9", "marketing_start_date": "20191227"}], "brand_name": "Carvedilol", "product_id": "68788-7539_ec264427-b2b2-4da7-94d6-18fdd7eaffd7", "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": "68788-7539", "generic_name": "Carvedilol", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "12.5 mg/1"}], "application_number": "ANDA077614", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}