Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 071489
Company: SUN PHARM INDUSTRIES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE 120MG TABLET;ORAL Discontinued None No No
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE 80MG 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
01/13/1988 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
05/16/2000 SUPPL-14 Manufacturing (CMC)-Facility

Label is not available on this site.

05/16/2000 SUPPL-13 Manufacturing (CMC)-Facility

Label is not available on this site.

08/05/1998 SUPPL-12 Labeling

Label is not available on this site.

12/05/1997 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

02/24/1997 SUPPL-10 Manufacturing (CMC)

Label is not available on this site.

04/24/1996 SUPPL-9 Labeling

Label is not available on this site.

06/22/1995 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

10/10/1995 SUPPL-7 Labeling

Label is not available on this site.

01/12/1994 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

06/29/1993 SUPPL-5 Labeling

Label is not available on this site.

10/24/1990 SUPPL-4 Labeling

Label is not available on this site.

04/04/1990 SUPPL-3 Labeling

Label is not available on this site.

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