NDC 55111-332

Pantoprazole

Pantoprazole

Pantoprazole is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Dr.reddy's Laboratories Limited. The primary component is Pantoprazole Sodium.

Product ID55111-332_02f0a994-cbaa-6f9b-56bd-48e9952540ec
NDC55111-332
Product TypeHuman Prescription Drug
Proprietary NamePantoprazole
Generic NamePantoprazole
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2011-01-19
Marketing CategoryANDA / ANDA
Application NumberANDA077619
Labeler NameDr.Reddy's Laboratories Limited
Substance NamePANTOPRAZOLE SODIUM
Active Ingredient Strength20 mg/1
Pharm ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 55111-332-01

100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-01)
Marketing Start Date2011-01-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55111-332-79 [55111033279]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-05 [55111033205]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-10 [55111033210]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-81 [55111033281]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-30 [55111033230]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-78 [55111033278]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-01 [55111033201]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-01-19

NDC 55111-332-90 [55111033290]

Pantoprazole TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077619
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-01-19

Drug Details

Active Ingredients

IngredientStrength
PANTOPRAZOLE SODIUM20 mg/1

OpenFDA Data

SPL SET ID:564709e8-358f-c185-4ecb-b3849c3fe59c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314200
  • 251872
    • UPC Code
  • 0068950000037

    • Pharmacological Class

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

    Medicade Reported Pricing

    55111033290 PANTOPRAZOLE SOD DR 20 MG TAB

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    53808-1007PantoprazolePantoprazole
    53808-1081PantoprazolePantoprazole
    55111-332PantoprazolePantoprazole
    55111-333PantoprazolePantoprazole
    60760-574PantoprazolePantoprazole
    31722-712PANTOPRAZOLE SODIUMPANTOPRAZOLE
    31722-713PANTOPRAZOLE SODIUMPANTOPRAZOLE
    42708-104PANTOPRAZOLE SODIUMPANTOPRAZOLE
    43353-569Pantoprazole SodiumPantoprazole
    45865-130PANTOPRAZOLE SODIUMPANTOPRAZOLE
    45865-676Pantoprazole SodiumPantoprazole
    50090-5793PANTOPRAZOLE SODIUMPANTOPRAZOLE
    50090-5794PANTOPRAZOLE SODIUMPANTOPRAZOLE
    50436-0712PANTOPRAZOLE SODIUMPANTOPRAZOLE
    55700-790PANTOPRAZOLE SODIUMPANTOPRAZOLE
    55700-850PANTOPRAZOLE SODIUMPANTOPRAZOLE
    60760-679PANTOPRAZOLE SODIUMPANTOPRAZOLE
    60760-712PANTOPRAZOLE SODIUMPANTOPRAZOLE
    63187-654PANTOPRAZOLE SODIUMPANTOPRAZOLE
    63187-831PANTOPRAZOLE SODIUMPANTOPRAZOLE
    63187-837Pantoprazole SodiumPantoprazole
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