NDC 71335-0881 – Amiodarone Hydrochloride

Amiodarone Hydrochloride 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0881

Product details

Brand name
Amiodarone Hydrochloride
Generic name
Amiodarone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075424
Marketed since
March 30, 2001
Listing expires
December 31, 2027
Pharmacologic class
Antiarrhythmic

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-0881-1200 TABLET in 1 BOTTLE (71335-0881-1)Dec 27, 2021
71335-0881-230 TABLET in 1 BOTTLE (71335-0881-2)Jan 3, 2019
71335-0881-360 TABLET in 1 BOTTLE (71335-0881-3)Dec 27, 2021
71335-0881-490 TABLET in 1 BOTTLE (71335-0881-4)Jun 26, 2018
71335-0881-510 TABLET in 1 BOTTLE (71335-0881-5)Dec 27, 2021

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