NDC 80425-0162

Protonix

Pantoprazole 40mg

Protonix is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Pantoprazole Sodium.

Product ID80425-0162_c950483e-33f9-bf0f-e053-2995a90afdd7
NDC80425-0162
Product TypeHuman Prescription Drug
Proprietary NameProtonix
Generic NamePantoprazole 40mg
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2014-09-10
Marketing CategoryANDA /
Application NumberANDA202882
Labeler NameAdvanced Rx Pharmacy of Tennessee, LLC
Substance NamePANTOPRAZOLE SODIUM
Active Ingredient Strength40 mg/1
Pharm ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 80425-0162-3

90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-3)
Marketing Start Date2014-09-10
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Protonix" or generic name "Pantoprazole 40mg"

NDCBrand NameGeneric Name
0008-0841ProtonixPANTOPRAZOLE SODIUM
0008-0843ProtonixPANTOPRAZOLE SODIUM
0008-0844ProtonixPANTOPRAZOLE SODIUM
0008-0923ProtonixPANTOPRAZOLE SODIUM
0008-0941Protonixpantoprazole sodium
0008-2001ProtonixPANTOPRAZOLE SODIUM
0008-4001ProtonixPANTOPRAZOLE SODIUM
21695-108Protonixpantoprazoel sodium
55154-4225Protonixpantoprazole sodium
55154-4232Protonixpantoprazole sodium
55154-4234Protonixpantoprazole sodium
55154-4236ProtonixPANTOPRAZOLE SODIUM
80425-0085ProtonixProtonix

Trademark Results [Protonix]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PROTONIX
PROTONIX
78263285 2836672 Dead/Cancelled
TAKEDA GMBH
2003-06-17
PROTONIX
PROTONIX
75391201 2207706 Live/Registered
TAKEDA GMBH
1997-11-17

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