Package 50742-363-60
Brand: ivabradine
Generic: ivabradinePackage Facts
Identity
Package NDC
50742-363-60
Digits Only
5074236360
Product NDC
50742-363
Description
60 TABLET, FILM COATED in 1 BOTTLE (50742-363-60)
Marketing
Marketing Status
Brand
ivabradine
Generic
ivabradine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6d23c13f-f81d-4bc9-9ded-be94c025e8f7", "openfda": {"upc": ["0350742363605", "0350742362608"], "unii": ["TP19837BZK"], "rxcui": ["1649485", "1649493"], "spl_set_id": ["2e70f883-8c01-4ac2-815d-4a6d561c711a"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50742-363-60)", "package_ndc": "50742-363-60", "marketing_start_date": "20240715"}], "brand_name": "IVABRADINE", "product_id": "50742-363_6d23c13f-f81d-4bc9-9ded-be94c025e8f7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Hyperpolarization-activated Cyclic Nucleotide-gated Channel Antagonists [MoA]", "Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker [EPC]"], "product_ndc": "50742-363", "generic_name": "IVABRADINE", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IVABRADINE", "active_ingredients": [{"name": "IVABRADINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA214051", "marketing_category": "ANDA", "marketing_start_date": "20240715", "listing_expiration_date": "20261231"}