Amiodarone Hydrochloride (Page 6 of 6)

Package/Label Display Panel

Amiodarone Hydrochloride Tablets

200 mg

10 Tablets

bag label
(click image for full-size original)
AMIODARONE HYDROCHLORIDE amiodarone hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55154-7890(NDC:0904-6556)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMIODARONE HYDROCHLORIDE (AMIODARONE) AMIODARONE HYDROCHLORIDE 200 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
POVIDONE, UNSPECIFIED
STARCH, CORN
Product Characteristics
Color WHITE (WHITE TO OFF- WHITE) Score 2 pieces
Shape ROUND (ROUND) Size 10mm
Flavor Imprint Code ZE;65
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:55154-7890-0 10 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 1 TABLET in 1 BLISTER PACK This package is contained within the CARTON (55154-7890-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA079029 08/10/2009 10/31/2020
Labeler — Cardinal Health (603638201)

Revised: 05/2020 Cardinal Health

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