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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017020
Company: ABBOTT
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PANWARFIN WARFARIN SODIUM 2MG TABLET;ORAL Discontinued None No No
PANWARFIN WARFARIN SODIUM 2.5MG TABLET;ORAL Discontinued None No No
PANWARFIN WARFARIN SODIUM 5MG TABLET;ORAL Discontinued None No No
PANWARFIN WARFARIN SODIUM 7.5MG TABLET;ORAL Discontinued None No No
PANWARFIN WARFARIN SODIUM 10MG 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
08/11/1972 ORIG-1 Approval Type 5 - New Formulation or New Manufacturer STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
02/25/1987 SUPPL-12 Labeling

Label is not available on this site.

09/25/1984 SUPPL-11 Manufacturing (CMC)-Formulation

Label is not available on this site.

06/29/1982 SUPPL-10 Manufacturing (CMC)-Control

Label is not available on this site.

09/26/1980 SUPPL-8 Labeling

Label is not available on this site.

03/30/1979 SUPPL-7 Manufacturing (CMC)-Control

Label is not available on this site.

01/11/1979 SUPPL-6 Manufacturing (CMC)-Control

Label is not available on this site.

04/28/1976 SUPPL-4 Labeling

Label is not available on this site.

12/12/1975 SUPPL-3 Labeling

Label is not available on this site.

06/23/1975 SUPPL-2 Manufacturing (CMC)-Control

Label is not available on this site.

03/03/1975 SUPPL-1 Unspecified

Label is not available on this site.

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