Package 60687-862-21

Brand: ivabradine

Generic: ivabradine
NDC Package

Package Facts

Identity

Package NDC 60687-862-21
Digits Only 6068786221
Product NDC 60687-862
Description

30 BLISTER PACK in 1 CARTON (60687-862-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-862-11)

Marketing

Marketing Status
Marketed Since 2025-07-01
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": "38e0b27f-e2e8-d69e-e063-6394a90a21dd", "openfda": {"unii": ["TP19837BZK"], "rxcui": ["1649485"], "spl_set_id": ["e881a1ac-9221-4682-939f-966679cfe286"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-862-21)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-862-11)", "package_ndc": "60687-862-21", "marketing_start_date": "20250701"}], "brand_name": "Ivabradine", "product_id": "60687-862_38e0b27f-e2e8-d69e-e063-6394a90a21dd", "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": "60687-862", "generic_name": "Ivabradine", "labeler_name": "American Health Packaging", "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": "20250701", "listing_expiration_date": "20261231"}