NDC 71335-1165

Pantoprazole Sodium

Pantoprazole Sodium

Pantoprazole Sodium is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Pantoprazole Sodium.

Product ID71335-1165_01ce3e07-8020-4947-8abe-8d71afe8fdd8
NDC71335-1165
Product TypeHuman Prescription Drug
Proprietary NamePantoprazole Sodium
Generic NamePantoprazole Sodium
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2012-09-28
Marketing CategoryANDA / ANDA
Application NumberANDA202038
Labeler NameBryant Ranch Prepack
Substance NamePANTOPRAZOLE SODIUM
Active Ingredient Strength20 mg/1
Pharm ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71335-1165-1

60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-1)
Marketing Start Date2013-10-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1165-8 [71335116508]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-10-14

NDC 71335-1165-6 [71335116506]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-10-14

NDC 71335-1165-5 [71335116505]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-10-14

NDC 71335-1165-4 [71335116504]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-10-14

NDC 71335-1165-1 [71335116501]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-10-14

NDC 71335-1165-3 [71335116503]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-10-14

NDC 71335-1165-2 [71335116502]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-10-14

NDC 71335-1165-7 [71335116507]

Pantoprazole Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA202038
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-10-14

Drug Details

Active Ingredients

IngredientStrength
PANTOPRAZOLE SODIUM20 mg/1

OpenFDA Data

SPL SET ID:9a1159d3-b9fa-4026-962c-d3001002e610
Manufacturer
UNII

Pharmacological Class

  • Proton Pump Inhibitor [EPC]
  • Proton Pump Inhibitors [MoA]
  • Proton Pump Inhibitor [EPC]
  • Proton Pump Inhibitors [MoA]

NDC Crossover Matching brand name "Pantoprazole Sodium" or generic name "Pantoprazole Sodium"

NDCBrand NameGeneric Name
0093-0011Pantoprazole SodiumPantoprazole Sodium
0093-0012Pantoprazole SodiumPantoprazole Sodium
0143-9284Pantoprazole SodiumPantoprazole Sodium
68071-1963Pantoprazole SodiumPantoprazole Sodium
68071-3038PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM
68071-1571Pantoprazole SodiumPantoprazole Sodium
68071-2082Pantoprazole SodiumPantoprazole Sodium
68071-2195Pantoprazole SodiumPantoprazole Sodium
68071-3140Pantoprazole SodiumPantoprazole Sodium
68071-3373Pantoprazole SodiumPantoprazole Sodium
68071-3334Pantoprazole SodiumPantoprazole Sodium
68071-4211Pantoprazole SodiumPantoprazole Sodium
68071-4483Pantoprazole SodiumPantoprazole Sodium
68071-4646Pantoprazole SodiumPantoprazole Sodium
68071-4347Pantoprazole SodiumPantoprazole Sodium
68084-643Pantoprazole SodiumPantoprazole Sodium
68084-813Pantoprazole SodiumPantoprazole Sodium
68645-491Pantoprazole SodiumPantoprazole Sodium
68645-492Pantoprazole SodiumPantoprazole Sodium
68788-6326Pantoprazole SodiumPantoprazole Sodium
68788-9263Pantoprazole SodiumPantoprazole Sodium
68788-9557PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM
68788-9660Pantoprazole SodiumPantoprazole Sodium
68788-9254Pantoprazole SodiumPantoprazole Sodium
68788-9510Pantoprazole SodiumPantoprazole Sodium
68788-9419Pantoprazole SodiumPantoprazole Sodium
70332-301Pantoprazole SodiumPantoprazole Sodium
70332-300PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM
70518-0226Pantoprazole SodiumPantoprazole Sodium
70518-0012Pantoprazole SodiumPantoprazole Sodium
70518-0395Pantoprazole SodiumPantoprazole Sodium
70518-0286Pantoprazole SodiumPantoprazole Sodium
70518-0860Pantoprazole SodiumPantoprazole Sodium
70518-0962Pantoprazole SodiumPantoprazole Sodium
70518-1298Pantoprazole SodiumPantoprazole Sodium
70518-1264Pantoprazole SodiumPantoprazole Sodium
70518-1788Pantoprazole SodiumPantoprazole Sodium
70934-203Pantoprazole SodiumPantoprazole Sodium
70934-145Pantoprazole SodiumPantoprazole Sodium
71335-0310Pantoprazole SodiumPantoprazole Sodium
71335-0476Pantoprazole SodiumPantoprazole Sodium
71335-0715Pantoprazole SodiumPantoprazole Sodium
71335-0291Pantoprazole SodiumPantoprazole Sodium
71610-003Pantoprazole SodiumPantoprazole Sodium
71335-0212Pantoprazole SodiumPantoprazole Sodium
71610-103Pantoprazole SodiumPantoprazole Sodium
71610-227Pantoprazole SodiumPantoprazole Sodium
71610-099Pantoprazole SodiumPantoprazole Sodium
0615-7629Pantoprazole SodiumPantoprazole Sodium
0615-7916Pantoprazole SodiumPantoprazole Sodium

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