Alembic Pharmaceuticals Limited today announced that it has received final approval from the USFDA for its ANDA for Doxycycline Hyclate Delayed-Release Tablets USP, 75 mg, 100 mg, 150 mg, and 200 mg.
NEW DELHI, Jan 4: Alembic Pharmaceuticals on Tuesday said it has received approval from the US health regulator to market Doxycycline Hyclate delayed-release tablets, used to treat drug resistant bacterial infections, in the American market. The company has received approval from the US Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Doxycycline Hyclate delayed-release tablets, the drug firm said in regulatory filing. The approved ANDA is therapeutically equivalent to the reference-listed drug product (RLD) Doryx […]