Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 076363
Company: SUN PHARM INDS INC

Products on ANDA 076363

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DIGOXIN	DIGOXIN	0.125MG	TABLET;ORAL	Discontinued	None	No	No
DIGOXIN	DIGOXIN	0.25MG	TABLET;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 076363

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
01/31/2003	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
10/07/2020	SUPPL-32	Labeling-Package Insert		Label is not available on this site.
10/07/2020	SUPPL-30	Labeling-Package Insert		Label is not available on this site.
10/07/2020	SUPPL-26	Labeling-Package Insert		Label is not available on this site.
10/07/2020	SUPPL-25	Labeling-Container/Carton Labels		Label is not available on this site.
10/07/2020	SUPPL-22	Labeling-Package Insert		Label is not available on this site.
10/07/2020	SUPPL-19	Labeling-Package Insert		Label is not available on this site.
07/06/2010	SUPPL-12	Labeling		Label is not available on this site.
06/14/2007	SUPPL-8	Manufacturing (CMC)-Control		Label is not available on this site.