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Dr. Reddy's Laboratories Ltd gets Form 483 with 4 observations from USFDA for Srikakulam formulations facility

The USFDA has completed a product-specific Pre-Approval Inspection and a routine GMP inspection at our formulations manufacturing facility in Srikakulam and issued a Form 483 with four observations. ....

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Dr. Reddy's Laboratories announces the launch of Regadenoson Injection 0.4 mg/5 mL in the U.S.

Dr. Reddy s Laboratories Ltd, today announced the launch of Regadenoson Injection in the U.S. market, approved by USFDA. ....

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Dr. Reddy's Laboratories Limited updates on USFDA GMP inspection at Bollaram unit

Dr. Reddy s Laboratories Limited has announced that the USFDA today completed a routine GMP inspection at the API manufacturing facility - CTO 1 in Bollaram, Hyderabad. ....

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Dr. Reddy's Laboratories announces the launch of Treprostinil Injection in the U.S.

Dr. Reddy s Laboratories Ltd today announced the launch of Treprostinil Injection in the U.S. market, a therapeutic equivalent generic version of Remodulin® Injection, approved by USFDA. ....

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