PRITI INDUSTRIES

Overview

PRITI INDUSTRIES is an active pharmaceutical ingredient (API) supplier with 13 active FDA Type II Drug Master Files, covering ALMAGATE EP/BP; ALUMINIUM HYDROXIDE MAGNESIUM CARBONATE CO-DRIED GEL; CALCIUM SILICATE USP; DRIED ALUMINIUM HYDROXIDE GEL IP/BP/USP; Hydrotalcite BP; LIGHT MAGNESIUM CARBONATE IP/BP/USP.

API / Drug Master Files

PRITI INDUSTRIES holds 13 active (13 total) FDA Type II Drug Master Files — identifying it as an active-substance / API supplier. Type II DMFs are filed with the FDA to support the use of an active pharmaceutical ingredient in drug applications.

• MAGNESIUM SILICATE USPActive2023-12-06
• LIGHT MAGNESIUM CARBONATE IP/BP/USPActive2023-12-06
• MAGNESIUM ALUMINIUM SILICATE HYDRATEActive2023-12-06
• Hydrotalcite BPActive2023-12-06
• MAGNESIUM ALUMINIUM METASILICATE USPActive2023-12-06
• CALCIUM SILICATE USPActive2023-12-06
• MAGALDRATE IP/BP/USPActive2023-12-06
• MAGNESIUM HYDROXIDE IP/BP/USPActive2023-11-18
• ALMAGATE EP/BPActive2023-11-18
• MAGNESIUM TRISILICATE IP/BP/USPActive2023-11-18
• DRIED ALUMINIUM HYDROXIDE GEL IP/BP/USPActive2023-11-18
• ALUMINIUM HYDROXIDE MAGNESIUM CARBONATE CO-DRIED GELActive2023-11-18
• MAGNESIUM HYDROXIDE PASTE USPActive2023-11-18

FDA compliance signals

No FDA recalls, Warning Letters, or Form 483 observations are linked to PRITI INDUSTRIES in our records. PharmaTek screens the full directory against live FDA enforcement data.