Alembic announces USFDA final approval for Pantoprazole Sodium for Injection, 40 mg/vial

Alembic announces USFDA final approval for Pantoprazole Sodium for Injection, 40 mg/vial

By: IPP Bureau

Last updated : April 03, 2025 10:59 am



Pantoprazole Sodium for Injection, 40 mg/vial (Single-Dose Vial) have an estimated market size of US$ 48 million for twelve months ending December 2024 according to IQVIA


Alembic Pharmaceuticals Limited (Alembic) announced that it has received Final Approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Pantoprazole Sodium for Injection, 40 mg/vial (Single-Dose Vial).

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Protonix I.V. for Injection, 40 mg/vial, of Wyeth Pharmaceuticals LLC. Pantoprazole sodium for injection is indicated for treatment of gastroesophageal reflux disease (GERD) and a history of erosive esophagitis (EE) for up to 10 days in adults.

It is also indicated for the treatment of pathological hypersecretion conditions including Zollinger-Ellison (ZE) Syndrome in adults. Refer label for a detailed indication.

Pantoprazole Sodium for Injection, 40 mg/vial (Single-Dose Vial) have an estimated market size of US$ 48 million for twelve months ending December 2024 according to IQVIA.

Alembic Pharmaceuticals Limited USFDA Pantoprazole Sodium

First Published : April 03, 2025 12:00 am