amiodarone hydrochloride
Generic: amiodarone hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
amiodarone hydrochloride
Generic Name
amiodarone hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
amiodarone hydrochloride 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1985
Product ID
71335-1985_84684b63-4bba-483c-a253-c67cc80d8276
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078578
Listing Expiration
2026-12-31
Marketing Start
2020-03-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351985
Hyphenated Format
71335-1985
Supplemental Identifiers
RxCUI
UNII
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
ANDA078578 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 200 TABLET in 1 BOTTLE (71335-1985-1)
- 30 TABLET in 1 BOTTLE (71335-1985-2)
- 60 TABLET in 1 BOTTLE (71335-1985-3)
- 90 TABLET in 1 BOTTLE (71335-1985-4)
- 10 TABLET in 1 BOTTLE (71335-1985-5)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "84684b63-4bba-483c-a253-c67cc80d8276", "openfda": {"unii": ["976728SY6Z"], "rxcui": ["833528"], "spl_set_id": ["f4532f12-3b7a-42ab-9a6c-36fd2a3f192c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (71335-1985-1)", "package_ndc": "71335-1985-1", "marketing_start_date": "20221013"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1985-2)", "package_ndc": "71335-1985-2", "marketing_start_date": "20221013"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1985-3)", "package_ndc": "71335-1985-3", "marketing_start_date": "20221013"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1985-4)", "package_ndc": "71335-1985-4", "marketing_start_date": "20211029"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1985-5)", "package_ndc": "71335-1985-5", "marketing_start_date": "20221013"}], "brand_name": "Amiodarone Hydrochloride", "product_id": "71335-1985_84684b63-4bba-483c-a253-c67cc80d8276", "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": "71335-1985", "generic_name": "Amiodarone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiodarone Hydrochloride", "active_ingredients": [{"name": "AMIODARONE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA078578", "marketing_category": "ANDA", "marketing_start_date": "20200309", "listing_expiration_date": "20261231"}