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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 208842
Company: SUN PHARMA CANADA

Products on ANDA 208842

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
CLOBETASOL PROPIONATE	CLOBETASOL PROPIONATE	0.05%	SPRAY;TOPICAL	Prescription	AT	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 208842

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
03/26/2018	ORIG-1	Approval		STANDARD		Label is not available on this site.

Therapeutic Equivalents for ANDA 208842

CLOBETASOL PROPIONATE

SPRAY;TOPICAL; 0.05%
TE Code = AT

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
CLOBETASOL PROPIONATE	CLOBETASOL PROPIONATE	0.05%	SPRAY;TOPICAL	Prescription	No	AT	211191	ALEMBIC
CLOBETASOL PROPIONATE	CLOBETASOL PROPIONATE	0.05%	SPRAY;TOPICAL	Prescription	No	AT	208842	SUN PHARMA CANADA
CLOBETASOL PROPIONATE	CLOBETASOL PROPIONATE	0.05%	SPRAY;TOPICAL	Prescription	No	AT	206378	ZYDUS PHARMS
CLOBEX	CLOBETASOL PROPIONATE	0.05%	SPRAY;TOPICAL	Prescription	Yes	AT	021835	GALDERMA LABS LP

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