amiodarone hydrochloride
Generic: amiodarone hydrochloride
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
amiodarone hydrochloride
Generic Name
amiodarone hydrochloride
Labeler
zydus lifesciences limited
Dosage Form
TABLET
Routes
Active Ingredients
amiodarone hydrochloride 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
65841-631
Product ID
65841-631_aabb5533-5d41-49a3-b8b6-14627af57311
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079029
Listing Expiration
2026-12-31
Marketing Start
2009-08-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65841631
Hyphenated Format
65841-631
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA079029 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 500 TABLET in 1 BOTTLE (65841-631-05)
- 30 TABLET in 1 BOTTLE (65841-631-06)
- 1000 TABLET in 1 BOTTLE (65841-631-10)
- 60 TABLET in 1 BOTTLE (65841-631-14)
- 10 BLISTER PACK in 1 CARTON (65841-631-77) / 10 TABLET in 1 BLISTER PACK
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aabb5533-5d41-49a3-b8b6-14627af57311", "openfda": {"unii": ["976728SY6Z"], "rxcui": ["833528", "834348", "835956"], "spl_set_id": ["3e8db251-e3c5-4fba-be9a-6044a92f0beb"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (65841-631-05)", "package_ndc": "65841-631-05", "marketing_start_date": "20090810"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65841-631-06)", "package_ndc": "65841-631-06", "marketing_start_date": "20090810"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65841-631-10)", "package_ndc": "65841-631-10", "marketing_start_date": "20090810"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65841-631-14)", "package_ndc": "65841-631-14", "marketing_start_date": "20090810"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65841-631-77) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "65841-631-77", "marketing_start_date": "20090810"}], "brand_name": "Amiodarone hydrochloride", "product_id": "65841-631_aabb5533-5d41-49a3-b8b6-14627af57311", "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": "65841-631", "generic_name": "Amiodarone hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiodarone hydrochloride", "active_ingredients": [{"name": "AMIODARONE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA079029", "marketing_category": "ANDA", "marketing_start_date": "20090810", "listing_expiration_date": "20261231"}