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Updated on: Tuesday, January 04, 2022, 12:20 PM IST

Alembic Pharma receives US FDA approval for doxycycline hyclate delayed-release tablets

Doxycycline Hyclate Delayed-Release tablets are indicated to reduce the development of drug-resistant bacteria.
The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Doryx Tablets, 75 mg,100 mg, 150 mg, and 200 mg./ Representative image |

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Doryx Tablets, 75 mg,100 mg, 150 mg, and 200 mg./ Representative image |

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Alembic Pharmaceuticals Limited announced that it has received final approval from the US Food & Drug Administration (US FDA) for its Abbreviated New Drug Application (ANDA) for Doxycycline Hyclate Delayed-Release Tablets USP, 75 mg, 100 mg, 150 mg, and 200 mg.

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Doryx Tablets, 75 mg,100 mg, 150 mg, and 200 mg, of Mayne Pharma International Pty. Ltd. (Mayne).

Doxycycline HyclateDelayed-Release Tablets are indicated to reduce the development of drug-resistant bacteria and maintain the effectiveness of Doxycycline HyclateDelayed-Release Tablets and other antibacterial drugs, Doxycycline HyclateDelayed-Release Tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.

Doxycycline Hyclate Delayed-Release Tablets USP, 75 mg, 100 mg, 150 mg, and 200 mg have an estimated market size of US$ 10 million for twelve months ending September 2021 according to IQVIA.

Alembic has received year to date (YTD) 16 approvals (12 final approvals and 4 tentative approvals) and a cumulative total of 155 ANDA approvals (135 final approvals and 20tentative approvals) from US FDA.

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Published on: Tuesday, January 04, 2022, 12:20 PM IST
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