ZOLOFT 
sertraline hydrochloride   tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0049-4900
Route of Administration ORAL DEA Schedule      
 
INGREDIENTS
Name (Active Moiety) Type Strength
sertraline hydrochloride (sertraline)  Active 50 MILLIGRAM  In 1 TABLET
dibasic calcium phosphate dihydrate Inactive  
FD & C Blue #2 aluminum lake Inactive  
hydroxypropyl cellulose Inactive  
hypromellose Inactive  
magnesium stearate Inactive  
microcrystalline cellulose Inactive  
polyethylene glycol Inactive  
polysorbate 80 Inactive  
sodium starch glycolate Inactive  
titanium dioxide Inactive  
 
Product Characteristics
Color blue (BLUE)  Score 2 pieces 
Shape OVAL (CAPSULE-SHAPED)  Size 10mm
Flavor  Imprint Code ZOLOFT;50;mg 
Contains     
Coating true Symbol false
 
Packaging
# NDC Package Description Multilevel Packaging
1 0049-4900-30 30 TABLET In 1 BOTTLE None
2 0049-4900-66 100 TABLET In 1 BOTTLE None
3 0049-4900-73 500 TABLET In 1 BOTTLE None
4 0049-4900-94 5000 TABLET In 1 BOTTLE None
5 0049-4900-41 100 TABLET In 1 DOSE PACK None

ZOLOFT 
sertraline hydrochloride   tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0049-4910
Route of Administration ORAL DEA Schedule      
 
INGREDIENTS
Name (Active Moiety) Type Strength
sertraline hydrochloride (sertraline)  Active 100 MILLIGRAM  In 1 TABLET
dibasic calcium phosphate dihydrate Inactive  
hydroxypropyl cellulose Inactive  
hypromellose Inactive  
magnesium stearate Inactive  
microcrystalline cellulose Inactive  
polyethylene glycol Inactive  
polysorbate 80 Inactive  
sodium starch glycolate Inactive  
synthetic yellow iron oxide Inactive  
titanium dioxide Inactive  
 
Product Characteristics
Color yellow (YE