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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 005657
Company: BRISTOL MYERS SQUIBB
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
TUBOCURARINE CHLORIDE TUBOCURARINE CHLORIDE 3MG/ML 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
02/20/1945 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
11/06/1992 SUPPL-10 Manufacturing (CMC)-Control

Label is not available on this site.

06/10/1987 SUPPL-9 Labeling

Label is not available on this site.

11/14/1986 SUPPL-8 Manufacturing (CMC)-Control

Label is not available on this site.

07/22/1985 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

08/19/1985 SUPPL-6 Labeling

Label is not available on this site.

07/28/1980 SUPPL-5 Manufacturing (CMC)-Control

Label is not available on this site.

04/29/1980 SUPPL-4 Labeling

Label is not available on this site.

02/16/1977 SUPPL-3 Labeling

Label is not available on this site.

12/16/1976 SUPPL-2 Labeling

Label is not available on this site.

11/28/1972 SUPPL-1 Labeling

Label is not available on this site.

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