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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 014738
Company: B BRAUN
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
MANNITOL 20% MANNITOL 20GM/100ML INJECTABLE;INJECTION 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
07/30/1964 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
10/07/2002 SUPPL-15 Manufacturing (CMC)-Microbiology-Processing

Label is not available on this site.

05/16/1985 SUPPL-13 Labeling

Label is not available on this site.

04/06/1985 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

07/09/1984 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

05/04/1981 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

09/11/1981 SUPPL-7 Labeling

Label is not available on this site.

05/24/1982 SUPPL-6 Labeling

Label is not available on this site.

05/28/1981 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

05/02/1979 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

08/10/1977 SUPPL-3 Labeling

Label is not available on this site.

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