Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017013
Company: ABBOTT
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
SODIUM CHLORIDE SODIUM CHLORIDE 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
10/08/1971 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
08/27/1996 SUPPL-18 Manufacturing (CMC)-Control

Label is not available on this site.

11/16/1982 SUPPL-16 Manufacturing (CMC)-Control

Label is not available on this site.

06/09/1982 SUPPL-15 Manufacturing (CMC)

Label is not available on this site.

04/21/1982 SUPPL-13 Labeling

Label is not available on this site.

12/11/1980 SUPPL-10 Manufacturing (CMC)-Packaging

Label is not available on this site.

08/12/1981 SUPPL-9 Labeling

Label is not available on this site.

01/19/1979 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

01/08/1979 SUPPL-6 Manufacturing (CMC)-Control

Label is not available on this site.

04/18/1979 SUPPL-4 Labeling

Label is not available on this site.

09/27/1976 SUPPL-3 Manufacturing (CMC)-Control

Label is not available on this site.

09/14/1976 SUPPL-2 Manufacturing (CMC)-Control

Label is not available on this site.

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