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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 091680
Company: LANNETT CO INC

Products on ANDA 091680

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DIETHYLPROPION HYDROCHLORIDE	DIETHYLPROPION HYDROCHLORIDE	75MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	Yes

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 091680

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
10/24/2011	ORIG-1	Approval	Not Applicable			Label is not available on this site.

Therapeutic Equivalents for ANDA 091680

DIETHYLPROPION HYDROCHLORIDE

TABLET, EXTENDED RELEASE;ORAL; 75MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
DIETHYLPROPION HYDROCHLORIDE	DIETHYLPROPION HYDROCHLORIDE	75MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	091680	LANNETT CO INC

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