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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 216654
Company: SOMERSET

Products on ANDA 216654

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
TIMOLOL	TIMOLOL	0.5%	SOLUTION/DROPS;OPHTHALMIC	Prescription	AT	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 216654

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
10/10/2024	ORIG-1	Approval		STANDARD		Label is not available on this site.

Therapeutic Equivalents for ANDA 216654

TIMOLOL

SOLUTION/DROPS;OPHTHALMIC; 0.5%
TE Code = AT

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
BETIMOL	TIMOLOL	0.5%	SOLUTION/DROPS;OPHTHALMIC	Prescription	Yes	AT	020439	THEA PHARMA
TIMOLOL	TIMOLOL	0.5%	SOLUTION/DROPS;OPHTHALMIC	Prescription	No	AT	216654	SOMERSET

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