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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 071133
Company: AIPING PHARM INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
HALOPERIDOL HALOPERIDOL 20MG 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
05/12/1987 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/09/1991 SUPPL-8 Labeling

Label is not available on this site.

05/09/1991 SUPPL-7 Labeling

Label is not available on this site.

03/19/1991 SUPPL-6 Labeling

Label is not available on this site.

10/25/1989 SUPPL-5 Labeling

Label is not available on this site.

02/23/1988 SUPPL-2 Labeling

Label is not available on this site.

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