Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 070100
Company: SUN PHARM INDUSTRIES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
FUROSEMIDE FUROSEMIDE 80MG TABLET;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
01/26/1988 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
12/01/1998 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

12/23/1994 SUPPL-10 Manufacturing (CMC)

Label is not available on this site.

10/11/1994 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

08/17/1993 SUPPL-8 Labeling

Label is not available on this site.

08/11/1992 SUPPL-7 Labeling

Label is not available on this site.

05/01/1992 SUPPL-6 Labeling

Label is not available on this site.

04/03/1992 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

04/03/1992 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

04/02/1991 SUPPL-2 Labeling

Label is not available on this site.

08/24/1988 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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