Strides gains USFDA approval for Theophylline Extended-Release Tablets, 300 mg and 450 mg

Strides is eligible for 180 days of Competitive Generic Therapy (CGT) exclusivity for Theophylline Extended-Release Tablets, 300 mg

Strides Pharma Science announced that its step-down wholly owned subsidiary, Strides Pharma Global, Singapore, has received approval for the generic version of Theophylline Extended-Release Tablets, 300 mg and 450 mg, from the United States Food and Drug Administration (USFDA). 

The product is bioequivalent and therapeutically equivalent to the Reference Listed Drug (RLD), THEO-DUR, of Schering Corp. Theophylline extended-release tablets are indicated for the treatment of symptoms and reversible airflow obstruction associated with chronic asthma and other chronic lung diseases, e.g., emphysema and chronic bronchitis. 

Theophylline Extended-Release Tablets, 300 mg and 450 mg have a combined market size of ~ $ 11.5 million, with the 300 mg dosage contributing ~ $ 10.8 million as per IQVIA. 

The Theophylline Extended-Release Tablets, 300 mg and 450 mg will be manufactured at the company’s flagship facility in KRS Gardens in Bengaluru, India. 

chronic bronchitischronic lung diseases medicationmphysemapharma newsSchering CorpStrides PharmaStrides Pharma Global SingaporeTheophylline Extended-Release TabletsUSFDA
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