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 ID | 80425-0162_c950483e-33f9-bf0f-e053-2995a90afdd7 |
NDC | 80425-0162 |
Product Type | Human Prescription Drug |
Proprietary Name | Protonix |
Generic Name | Pantoprazole 40mg |
Dosage Form | Tablet, Delayed Release |
Route of Administration | ORAL |
Marketing Start Date | 2014-09-10 |
Marketing Category | ANDA / |
Application Number | ANDA202882 |
Labeler Name | Advanced Rx Pharmacy of Tennessee, LLC |
Substance Name | PANTOPRAZOLE SODIUM |
Active Ingredient Strength | 40 mg/1 |
Pharm Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2014-09-10 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
0008-0841 | Protonix | PANTOPRAZOLE SODIUM |
0008-0843 | Protonix | PANTOPRAZOLE SODIUM |
0008-0844 | Protonix | PANTOPRAZOLE SODIUM |
0008-0923 | Protonix | PANTOPRAZOLE SODIUM |
0008-0941 | Protonix | pantoprazole sodium |
0008-2001 | Protonix | PANTOPRAZOLE SODIUM |
0008-4001 | Protonix | PANTOPRAZOLE SODIUM |
21695-108 | Protonix | pantoprazoel sodium |
55154-4225 | Protonix | pantoprazole sodium |
55154-4232 | Protonix | pantoprazole sodium |
55154-4234 | Protonix | pantoprazole sodium |
55154-4236 | Protonix | PANTOPRAZOLE SODIUM |
80425-0085 | Protonix | Protonix |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PROTONIX 78263285 2836672 Dead/Cancelled |
TAKEDA GMBH 2003-06-17 |
PROTONIX 75391201 2207706 Live/Registered |
TAKEDA GMBH 1997-11-17 |