Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 062413
Company: ABBOTT

Products on ANDA 062413

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 1.2MG BASE/ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 1.4MG BASE/ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 1.6MG BASE/ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 1.8MG BASE/ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 2MG BASE/ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 60MG BASE/100ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 70MG BASE/100ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 80MG BASE/100ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 90MG BASE/100ML	INJECTABLE;INJECTION	Discontinued	None	No	No
GENTAMICIN SULFATE	GENTAMICIN SULFATE	EQ 100MG BASE/100ML	INJECTABLE;INJECTION	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 062413

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
08/11/1983	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
07/14/1993	SUPPL-6	Labeling		Label is not available on this site.