amiodarone hydrochloride
Generic: amiodarone hydrochloride
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
amiodarone hydrochloride
Generic Name
amiodarone hydrochloride
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
amiodarone hydrochloride 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-616
Product ID
63323-616_262974e7-d551-4123-adfa-2ee1c4fa6195
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075761
Listing Expiration
2026-12-31
Marketing Start
2003-01-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323616
Hyphenated Format
63323-616
Supplemental Identifiers
RxCUI
UPC
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
ANDA075761 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-616-03) / 3 mL in 1 VIAL, SINGLE-DOSE (63323-616-01)
- 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-616-09) / 9 mL in 1 VIAL, SINGLE-DOSE (63323-616-02)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "262974e7-d551-4123-adfa-2ee1c4fa6195", "openfda": {"upc": ["0363323616021", "0363323616014"], "unii": ["976728SY6Z"], "rxcui": ["1663224", "1663244"], "spl_set_id": ["d8d04647-8e25-4127-8ecf-360ce1991c2f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (63323-616-03) / 3 mL in 1 VIAL, SINGLE-DOSE (63323-616-01)", "package_ndc": "63323-616-03", "marketing_start_date": "20030128"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (63323-616-09) / 9 mL in 1 VIAL, SINGLE-DOSE (63323-616-02)", "package_ndc": "63323-616-09", "marketing_start_date": "20030128"}], "brand_name": "Amiodarone Hydrochloride", "product_id": "63323-616_262974e7-d551-4123-adfa-2ee1c4fa6195", "dosage_form": "INJECTION, SOLUTION", "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": "63323-616", "generic_name": "AMIODARONE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiodarone Hydrochloride", "active_ingredients": [{"name": "AMIODARONE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA075761", "marketing_category": "ANDA", "marketing_start_date": "20030128", "listing_expiration_date": "20261231"}