DESMOPRESSIN ACETATE - desmopressin acetate spray 
Zydus Lifesciences Limited

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DESMOPRESSIN ACETATE NASAL SOLUTION (NASAL SPRAY)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1314-1

Desmopressin Acetate Nasal Solution (Nasal Spray), 10 mcg/ 0.1 mL per spray

5 mL

Rx only

Image
DESMOPRESSIN ACETATE 
desmopressin acetate spray
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1314
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DESMOPRESSIN ACETATE (UNII: XB13HYU18U) (DESMOPRESSIN - UNII:ENR1LLB0FP) DESMOPRESSIN ACETATE0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1314-15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09134502/01/2018
Labeler - Zydus Lifesciences Limited (918596198)
Registrant - Zydus Lifesciences Limited (918596198)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited918596198ANALYSIS(70771-1314) , MANUFACTURE(70771-1314)

Revised: 10/2022
Document Id: d7ff2b95-b76f-4587-a38a-4de57dd2c726
Set id: 80ee3c8b-0b8f-4261-bb64-a47c4c9b96bb
Version: 5
Effective Time: 20221031
 
Zydus Lifesciences Limited