Amiodarone Hydrochloride (Page 8 of 8)

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Label
(click image for full-size original)
AMIODARONE HYDROCHLORIDE
amiodarone hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-387(NDC:0185-0144)
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
SILICON DIOXIDE
STARCH, CORN
D&C YELLOW NO. 10
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
POVIDONES
Product Characteristics
Color YELLOW Score 2 pieces
Shape ROUND Size 10mm
Flavor Imprint Code E;144
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-387-10 10 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK
1 10 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (63739-387-10)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075315 12/23/1998
Labeler — McKesson Packaging Services a business unit of McKesson Corporation (140529962)
Registrant — McKesson Packaging Services a business unit of McKesson Corporation (140529962)
Establishment
Name Address ID/FEI Operations
McKesson Packaging Services a business unit of McKesson Corporation 140529962 REPACK (63739-387)

Revised: 10/2013 McKesson Packaging Services a business unit of McKesson Corporation

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