Ziprasidone Hydrochloride (Page 9 of 9)

ZIPRASIDONE HYDROCHLORIDE CAPSULE

Label ImageLabel Image
ZIPRASIDONE HYDROCHLORIDE ziprasidone hydrochloride capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-5420(NDC:33342-145)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZIPRASIDONE HYDROCHLORIDE (ZIPRASIDONE) ZIPRASIDONE 40 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
POLYETHYLENE GLYCOL, UNSPECIFIED
SODIUM STARCH GLYCOLATE TYPE A POTATO
AMMONIUM CHLORIDE
SUCROSE
SODIUM LAURYL SULFATE
SHELLAC
PROPYLENE GLYCOL
FERROSOFERRIC OXIDE
FD&C BLUE NO. 2
TITANIUM DIOXIDE
GELATIN, UNSPECIFIED
Product Characteristics
Color BLUE (blue coloured cap and body) Score no score
Shape CAPSULE (capsule) Size 18mm
Flavor Imprint Code CL63;40mg
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-5420-0 60 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA204375 02/18/2017
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-5420)

Revised: 01/2021 A-S Medication Solutions

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