NDC 70436-232 – Amiodarone Hydrochloride

Amiodarone Hydrochloride 50 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC70436-232

Product details

Brand name
Amiodarone Hydrochloride
Generic name
Amiodarone hydrochloride
Labeler
Slate Run Pharmaceuticals
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA218253
Marketed since
October 31, 2024
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Amiodarone Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
70436-232-501 VIAL in 1 CARTON (70436-232-50) / 18 mL in 1 VIALOct 31, 2024
70436-232-5210 VIAL in 1 CARTON (70436-232-52) / 3 mL in 1 VIALOct 31, 2024
70436-232-6210 VIAL in 1 CARTON (70436-232-62) / 9 mL in 1 VIALOct 31, 2024

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