Drugs@FDA: FDA Approved Drug Products

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New Drug Application (NDA): 017569
Company: GLENWOOD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
RENOQUID SULFACYTINE 250MG 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
09/12/1975 ORIG-1 Approval Type 1 - New Molecular Entity PRIORITY

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
12/16/1986 SUPPL-6 Labeling

Label is not available on this site.

04/09/1981 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

10/23/1979 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

07/05/1978 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

01/12/1978 SUPPL-2 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

11/22/1976 SUPPL-1 Manufacturing (CMC)-Packaging

Label is not available on this site.

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