BETAMETHASONE DIPROPIONATE - betamethasone dipropionate ointment 
Zydus Lifesciences Limited

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BETAMETHASONE DIPROPIONATE
OINTMENT USP, 0.05%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Betamethasone Dipropionate Ointment USP, 0.05%

NDC 70771-1550-1 in tube of 15 gm

Rx Only

tube label
carton label
BETAMETHASONE DIPROPIONATE 
betamethasone dipropionate ointment
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1550
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE0.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1550-11 in 1 CARTON07/20/2020
115 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:70771-1550-41 in 1 CARTON07/20/2020
245 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21404807/20/2020
Labeler - Zydus Lifesciences Limited (918596198)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited650650802ANALYSIS(70771-1550) , MANUFACTURE(70771-1550)

Revised: 11/2022
Document Id: 34685b34-d41c-4a8b-b6db-9cd17e4ced70
Set id: f531da27-2435-49a3-8992-c65240c6a7fe
Version: 3
Effective Time: 20221105
 
Zydus Lifesciences Limited