Drugs@FDA: FDA-Approved Drugs

Home | Previous Page

Abbreviated New Drug Application (ANDA): 207899
Company: TORRENT

Products on ANDA 207899

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
MOMETASONE FUROATE	MOMETASONE FUROATE	0.1%	OINTMENT;TOPICAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 207899

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
07/13/2018	ORIG-1	Approval		STANDARD		Label is not available on this site.

Therapeutic Equivalents for ANDA 207899

MOMETASONE FUROATE

OINTMENT;TOPICAL; 0.1%
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
MOMETASONE FUROATE	MOMETASONE FUROATE	0.1%	OINTMENT;TOPICAL	Prescription	No	AB	077401	COSETTE
MOMETASONE FUROATE	MOMETASONE FUROATE	0.1%	OINTMENT;TOPICAL	Prescription	No	AB	077061	FOUGERA PHARMS
MOMETASONE FUROATE	MOMETASONE FUROATE	0.1%	OINTMENT;TOPICAL	Prescription	No	AB	076067	PADAGIS US
MOMETASONE FUROATE	MOMETASONE FUROATE	0.1%	OINTMENT;TOPICAL	Prescription	No	AB	207899	TORRENT