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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 206173
Company: CADILA PHARMS LTD

Products on ANDA 206173

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	No
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	No
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 206173

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
05/05/2017	ORIG-1	Approval		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
03/27/2020	SUPPL-3	Labeling-Package Insert		Label is not available on this site.
09/25/2019	SUPPL-1	Labeling-Package Insert		Label is not available on this site.

Therapeutic Equivalents for ANDA 206173

VERAPAMIL HYDROCHLORIDE

TABLET, EXTENDED RELEASE;ORAL; 180MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	206173	CADILA PHARMS LTD
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	090700	GLENMARK GENERICS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	074330	IVAX SUB TEVA PHARMS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	090529	SUN PHARM INDS INC

TABLET, EXTENDED RELEASE;ORAL; 240MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	206173	CADILA PHARMS LTD
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	078906	GLENMARK GENERICS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	073568	IVAX SUB TEVA PHARMS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	075072	STRIDES PHARMA
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	090529	SUN PHARM INDS INC

TABLET, EXTENDED RELEASE;ORAL; 120MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	206173	CADILA PHARMS LTD
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	090700	GLENMARK GENERICS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	073568	IVAX SUB TEVA PHARMS
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	075072	STRIDES PHARMA
VERAPAMIL HYDROCHLORIDE	VERAPAMIL HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE;ORAL	Prescription	No	AB	090529	SUN PHARM INDS INC

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