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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 084631
Company: SANDOZ
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
QUINIDINE SULFATE QUINIDINE SULFATE 200MG 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
11/24/1976 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
02/02/2000 SUPPL-18 Manufacturing (CMC)-Facility

Label is not available on this site.

02/18/1999 SUPPL-17 Labeling

Label is not available on this site.

09/03/1996 SUPPL-16 Labeling

Label is not available on this site.

10/29/1992 SUPPL-15 Labeling

Label is not available on this site.

02/28/1995 SUPPL-14 Labeling

Label is not available on this site.

02/28/1995 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

02/05/1988 SUPPL-12 Labeling

Label is not available on this site.

03/12/1985 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

10/25/1983 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

10/25/1983 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

06/18/1982 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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