Package 31722-053-60

Brand: ivabradine

Generic: ivabradine
NDC Package

Package Facts

Identity

Package NDC 31722-053-60
Digits Only 3172205360
Product NDC 31722-053
Description

60 TABLET, FILM COATED in 1 BOTTLE (31722-053-60)

Marketing

Marketing Status
Marketed Since 2022-10-05
Brand ivabradine
Generic ivabradine
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "174dfa8e-391c-3a0d-e063-6294a90af7ca", "openfda": {"upc": ["0331722054607", "0331722053600"], "unii": ["TP19837BZK"], "rxcui": ["1649485", "1649493"], "spl_set_id": ["602d1c55-0e4d-452a-a087-888fdbaa7568"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-053-60)", "package_ndc": "31722-053-60", "marketing_start_date": "20221005"}], "brand_name": "Ivabradine", "product_id": "31722-053_174dfa8e-391c-3a0d-e063-6294a90af7ca", "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": "31722-053", "generic_name": "Ivabradine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ivabradine", "active_ingredients": [{"name": "IVABRADINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA213366", "marketing_category": "ANDA", "marketing_start_date": "20221005", "listing_expiration_date": "20261231"}