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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 204196
Company: SUN PHARM

Products on ANDA 204196

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE	DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE	20MG;10MG	CAPSULE;ORAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 204196

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
06/03/2026	ORIG-1	Approval		STANDARD		Label is not available on this site.

Therapeutic Equivalents for ANDA 204196

DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE

CAPSULE;ORAL; 20MG;10MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE	DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE	20MG;10MG	CAPSULE;ORAL	Prescription	No	AB	202934	ACTAVIS ELIZABETH
DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE	DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE	20MG;10MG	CAPSULE;ORAL	Prescription	No	AB	218426	HETERO LABS LTD III
DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE	DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE	20MG;10MG	CAPSULE;ORAL	Prescription	No	AB	204196	SUN PHARM
NUEDEXTA	DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE	20MG;10MG	CAPSULE;ORAL	Prescription	Yes	AB	021879	OTSUKA AMERICA PHARM

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