Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 072924
Company: WATSON LABS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE 40MG TABLET;ORAL Prescription AB 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
06/29/1993 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
10/26/2015 SUPPL-20 Labeling-Package Insert

Label is not available on this site.

11/26/2012 SUPPL-19 Labeling-Package Insert

Label is not available on this site.

04/19/2007 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

11/07/2002 SUPPL-9 Manufacturing (CMC)-Facility

Label is not available on this site.

06/25/2002 SUPPL-8 Manufacturing (CMC)-Control

Label is not available on this site.

05/21/2002 SUPPL-6 Manufacturing (CMC)-Facility

Label is not available on this site.

09/05/2001 SUPPL-5 Manufacturing (CMC)-Control

Label is not available on this site.

11/10/1999 SUPPL-4 Manufacturing (CMC)-Packaging

Label is not available on this site.

08/26/1998 SUPPL-3 Labeling

Label is not available on this site.

04/10/1996 SUPPL-2 Labeling

Label is not available on this site.

01/27/1994 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

VERAPAMIL HYDROCHLORIDE

TABLET;ORAL; 40MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE 40MG TABLET;ORAL Prescription No AB 071881 HERITAGE PHARMS INC
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE 40MG TABLET;ORAL Prescription No AB 072924 WATSON LABS

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