Sildenafil (Page 7 of 7)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sildenafil tablets 20 mg-90s count

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SILDENAFIL sildenafil tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72865-105
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SILDENAFIL CITRATE (SILDENAFIL) SILDENAFIL 20 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
HYPROMELLOSES
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
TITANIUM DIOXIDE
TRIACETIN
Product Characteristics
Color white Score no score
Shape ROUND Size 7mm
Flavor Imprint Code J;95
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:72865-105-90 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203623 07/10/2019
Labeler — XLCare Pharmaceuticals, Inc. (080991142)
Registrant — Evaric Pharmaceuticals Inc (080470330)
Establishment
Name Address ID/FEI Operations
Evaric Pharmaceuticals Inc 080470330 analysis (72865-105), manufacture (72865-105)

Revised: 01/2023 XLCare Pharmaceuticals, Inc.

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