Laurus Labs Limited
Anakapalli, India · makes it, makes the active ingredient and tests it
Problems found, fixed voluntarily Last FDA inspection Feb 10, 2023. 2 inspections on record.
NDC 51655-644
On the label: Northwind Pharmaceuticals.
It's a repackaged product: Northwind Pharmaceuticals rebottles it from Laurus Labs Limited's NDC 42385-949.
Anakapalli, India · makes it, makes the active ingredient and tests it
Problems found, fixed voluntarily Last FDA inspection Feb 10, 2023. 2 inspections on record.
51655-644-26 Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?