Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 200104
Company: AIPING PHARM INC

Products on ANDA 200104

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
WARFARIN SODIUM	WARFARIN SODIUM	1MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	2MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	2.5MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	3MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	4MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	5MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	6MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	7.5MG	TABLET;ORAL	Discontinued	None	No	No
WARFARIN SODIUM	WARFARIN SODIUM	10MG	TABLET;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 200104

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
06/27/2013	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
11/14/2019	SUPPL-5	Labeling-Medication Guide, Labeling-Package Insert		Label is not available on this site.
11/14/2019	SUPPL-4	Labeling-Medication Guide, Labeling-Package Insert		Label is not available on this site.
11/14/2019	SUPPL-2	Labeling-Medication Guide, Labeling-Package Insert		Label is not available on this site.
11/14/2019	SUPPL-1	Labeling-Package Insert		Label is not available on this site.