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According to IMS Health, Pantoprazole Sodium
Delayed-Released tablets recorded total US sales of approximately USD1.8bn for the 12 months ending 30 September 2010.
18 October 2010 - Canada-based pharmaceutical company Intellipharmaceutics International Inc (TSE: I) today announced that the Food and Drug Administration (FDA) has accepted for filing its abbreviated new drug application (ANDA) for a generic version of Protonix (delayed release pantoprazole sodium
Delayed-Release Tablets 20mg and 40mg, the generic equivalent of Protonix 20mg and 40mg by Pfizer (NYSE: PFE), had US sales of about USD1.6bn (EUR1.17bn) for the 12 months ending 31 December 2010, according to IMS Health.
The US Food and Drug Administration (FDA) has granted final approval for the Abbreviated New Drug Application (ANDA) for Pantoprazole Sodium
Delayed-release Tablets USP, 20 mg (base) and 40 mg (base).
Combination product of PAN and ITH (Label claim: Pantoprazole 40 mg, as pantoprazole sodium
sesquihydrate, and benazepril hydrochloride 150 mg), Itopan and Pantop-IT tablets (Alkem and Unichem Laboratories Ltd.) were purchased from the market.
Kremers Urban extended-release products that require complex drug development technology and manufacturing process include hydrocodone polistirex and chlorpheniramine polistirex pennkinetic extended-release suspension CIII (authorized generic for Tussionex Pennkinetic Extended-Release Suspension CIII), pantoprazole sodium
delayed-release tablets, oxybutynin chloride extended-release tablets USE omeprazole delayed-release capsules, nifedipine extended-release tablets USE verapamil hydrochloride extendedrelease capsules, and several other extendedrelease and transdermal generic products.