amiodarone hydrochloride

Generic: amiodarone hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amiodarone hydrochloride
Generic Name amiodarone hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amiodarone hydrochloride 200 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-4025
Product ID 51672-4025_4cc4c3cb-aced-a125-e063-6394a90aee93
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075424
Listing Expiration 2027-12-31
Marketing Start 2001-03-30

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724025
Hyphenated Format 51672-4025

Supplemental Identifiers

UPC
0351672405663 0351672405762 0351672405564
UNII
976728SY6Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name amiodarone hydrochloride (source: ndc)
Generic Name amiodarone hydrochloride (source: ndc)
Application Number ANDA075424 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (51672-4025-2)
  • 1000 TABLET in 1 BOTTLE (51672-4025-3)
  • 60 TABLET in 1 BOTTLE (51672-4025-4)
source: ndc

Packages (3)

51672-4025-2 500 TABLET in 1 BOTTLE (51672-4025-2) 51672-4025-3 1000 TABLET in 1 BOTTLE (51672-4025-3) 51672-4025-4 60 TABLET in 1 BOTTLE (51672-4025-4)

Ingredients (1)

amiodarone hydrochloride (200 mg/1)

Linked Drug Pages (1)

Amiodarone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4cc4c3cb-aced-a125-e063-6394a90aee93", "openfda": {"upc": ["0351672405663", "0351672405762", "0351672405564"], "unii": ["976728SY6Z"], "spl_set_id": ["7ccd3733-c3af-4a11-8500-0f99194c1472"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (51672-4025-2)", "package_ndc": "51672-4025-2", "marketing_start_date": "20010330"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4025-3)", "package_ndc": "51672-4025-3", "marketing_start_date": "20010330"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (51672-4025-4)", "package_ndc": "51672-4025-4", "marketing_start_date": "20010330"}], "brand_name": "Amiodarone Hydrochloride", "product_id": "51672-4025_4cc4c3cb-aced-a125-e063-6394a90aee93", "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": "51672-4025", "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": "200 mg/1"}], "application_number": "ANDA075424", "marketing_category": "ANDA", "marketing_start_date": "20010330", "listing_expiration_date": "20271231"}