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LEVITRA (vardenafil hydrochloride) tablets(三十)
2018-06-25 10:12:10 来源: 作者: 【 】 浏览:16695次 评论:0
FERRIC OXIDE RED (UNII: 1K09F3G675)   
Product Characteristics 
Color ORANGE Score no score 
Shape ROUND Size 6mm 
Flavor  Imprint Code BAYER;5 
Contains      
Packaging 
#
Item Code
Package Description
Marketing Start Date
Marketing End Date
1
NDC:0173-0829-13 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/23/2003  
Marketing Information 
Marketing Category
Application Number or Monograph Citation
Marketing Start Date
 
Marketing End Date
 
NDA NDA021400 04/23/2003  
LEVITRA  
vardenafil hydrochloride tablet, film coated 
 
Product Information 
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0173-0830 
Route of Administration ORAL 
Active Ingredient/Active Moiety 
 
Ingredient Name
 
Basis of Strength
 
Strength
 
VARDENAFIL HYDROCHLORIDE (UNII: 5M8S2CU0TS) (VARDENAFIL - UNII:UCE6F4125H) VARDENAFIL 10 mg 
Inactive Ingredients 
 
Ingredient Name
 
Strength
 
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)   
CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)   
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)   
MAGNESIUM STEARATE (UNII: 70097M6I30)   
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)   
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)   
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)   
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)   
FERRIC OXIDE RED (UNII: 1K09F3G675)   
Product Characteristics 
Color ORANGE Score no score 
Shape ROUND Size 7mm 
Flavor  Imprint Code BAYER;10 
Contains      
Packaging 
 
#
 
Item Code
 
Package Description
 
Marketing Start Date
 
Marketing End Date
1
NDC:0173-0830-13 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/25/2017  
 
2
NDC:0173-0830-61 1 in 1 CARTON 08/25/2003  
 
2
 2 in 1 BLISTER PACK; Type 0: Not a Combination Product   
 
Marketing Information 
 
Marketing Category
 
Application Number or Monograph Citation
 
Marketing Start Date
 
Marketing End Date
 
NDA NDA021400 08/25/2003  
LEVITRA  
vardenafil hydrochloride tablet, film coated 
 
Product Information 
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0173-0831 
Route of Administration ORAL 
Active Ingredient/Active Moiety 
 
Ingredient Name
 
Basis of Strength
 
Strength
 
VARDENAFIL HYDROCHLORIDE (UNII: 5M8S2CU0TS) (VARDENAFIL - UNII:UCE6F4125H) VARDENAFIL 20 mg 
 
Inactive Ingredients 
 
Ingredien
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