Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 018866
Company: FOUGERA PHARMS INC

Products on NDA 018866

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
BETAMETHASONE VALERATE	BETAMETHASONE VALERATE	EQ 0.1% BASE	LOTION;TOPICAL	Prescription	AB	Yes	Yes

Approval Date(s) and History, Letters, Labels, Reviews for NDA 018866

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
08/31/1983	ORIG-1	Approval				Label is not available on this site.

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
03/24/2014	SUPPL-13	Manufacturing (CMC)		Label is not available on this site.
12/12/1996	SUPPL-10	Labeling		Label is not available on this site.
04/14/1995	SUPPL-9	Manufacturing (CMC)		Label is not available on this site.
11/29/1988	SUPPL-8	Labeling		Label is not available on this site.
10/26/1988	SUPPL-7	Manufacturing (CMC)		Label is not available on this site.
10/26/1988	SUPPL-6	Manufacturing (CMC)		Label is not available on this site.
05/28/1987	SUPPL-5	Manufacturing (CMC)		Label is not available on this site.
05/28/1987	SUPPL-4	Manufacturing (CMC)		Label is not available on this site.

Therapeutic Equivalents for NDA 018866

BETAMETHASONE VALERATE

LOTION;TOPICAL; EQ 0.1% BASE
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
BETAMETHASONE VALERATE	BETAMETHASONE VALERATE	EQ 0.1% BASE	LOTION;TOPICAL	Prescription	No	AB	070052	ANIMA
BETAMETHASONE VALERATE	BETAMETHASONE VALERATE	EQ 0.1% BASE	LOTION;TOPICAL	Prescription	Yes	AB	018866	FOUGERA PHARMS INC