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NDC 70518-1939-01 Amiodarone Hydrochloride 200 mg/1 Details

Amiodarone Hydrochloride 200 mg/1

Amiodarone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is AMIODARONE HYDROCHLORIDE.

MedlinePlus Drug Summary

Amiodarone is used to treat and prevent certain types of serious, life-threatening ventricular arrhythmias (a certain type of abnormal heart rhythm when other medications did not help or could not be tolerated. Amiodarone is in a class of medications called antiarrhythmics. It works by relaxing overactive heart muscles.

Related Packages: 70518-1939-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Amiodarone

Product Information

NDC	70518-1939
Product ID	70518-1939_fe3f2602-d3ea-2bb2-e053-6294a90a6649
Associated GPIs	35400005000305
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Amiodarone Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Amiodarone Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	200
Active Ingredient Units	mg/1
Substance Name	AMIODARONE HYDROCHLORIDE
Labeler Name	REMEDYREPACK INC.
Pharmaceutical 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]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA204742
Listing Certified Through	2024-12-31

Package

NDC 70518-1939-01 (70518193901)

Pricing Information	N/A
NDC Package Code	70518-1939-1
Billing NDC	70518193901
Package	90 TABLET in 1 BOTTLE, PLASTIC (70518-1939-1)
Marketing Start Date	2021-02-23
NDC Exclude Flag	N