Package 51672-4056-6
Brand: amiodarone hydrochloride
Generic: amiodarone hydrochloridePackage Facts
Identity
Package NDC
51672-4056-6
Digits Only
5167240566
Product NDC
51672-4056
Description
30 TABLET in 1 BOTTLE (51672-4056-6)
Marketing
Marketing Status
Brand
amiodarone hydrochloride
Generic
amiodarone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31e40baa-ae5a-8747-e063-6294a90acd07", "openfda": {"upc": ["0351672405663", "0351672405762", "0351672405564"], "unii": ["976728SY6Z"], "rxcui": ["833528", "834348", "835956", "835960"], "spl_set_id": ["7ccd3733-c3af-4a11-8500-0f99194c1472"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (51672-4056-0) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "51672-4056-0", "marketing_start_date": "20031202"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4056-1)", "package_ndc": "51672-4056-1", "marketing_start_date": "20031202"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4056-3)", "package_ndc": "51672-4056-3", "marketing_start_date": "20031202"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51672-4056-6)", "package_ndc": "51672-4056-6", "marketing_start_date": "20031202"}], "brand_name": "Amiodarone Hydrochloride", "product_id": "51672-4056_31e40baa-ae5a-8747-e063-6294a90acd07", "dosage_form": "TABLET", "pharm_class": ["Antiarrhythmic [EPC]", "Cytochrome P450 1A2 Inhibitors [MoA]", "Cytochrome P450 2C9 Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]", "Cytochrome P450 3A Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "51672-4056", "generic_name": "Amiodarone Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiodarone Hydrochloride", "active_ingredients": [{"name": "AMIODARONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA076362", "marketing_category": "ANDA", "marketing_start_date": "20031202", "listing_expiration_date": "20261231"}