Stavudine (Page 9 of 9)

PACKAGE LABEL

Label Image for 53808-0852 20mg

Label Image for 20mgLabel Image for 20mg
STAVUDINE stavudine capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0852(NDC:0378-5041)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STAVUDINE (STAVUDINE) STAVUDINE 20 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
SODIUM STARCH GLYCOLATE TYPE A POTATO
D&C RED NO. 28
FD&C BLUE NO. 1
FD&C RED NO. 40
GELATIN
TITANIUM DIOXIDE
FERROSOFERRIC OXIDE
POTASSIUM HYDROXIDE
PROPYLENE GLYCOL
SHELLAC
Product Characteristics
Color PINK (pink opaque) Score no score
Shape CAPSULE Size 18mm
Flavor Imprint Code M;155
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0852-1 30 CAPSULE (CAPSULE) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA079069 01/01/2013
Labeler — State of Florida DOH Central Pharmacy (829348114)
Establishment
Name Address ID/FEI Operations
State of Florida DOH Central Pharmacy 829348114 repack (53808-0852)

Revised: 09/2013 State of Florida DOH Central Pharmacy

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