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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 087541
Company: ASCOT

Products on ANDA 087541

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
TOLBUTAMIDE	TOLBUTAMIDE	500MG	TABLET;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 087541

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
10/05/1983	SUPPL-1	Manufacturing (CMC)		Label is not available on this site.

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