NDC 68071-2891

Pantoprazole

Pantoprazole

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

Product ID68071-2891_eeb5f3b4-5e6f-8bec-e053-2995a90a6457
NDC68071-2891
Product TypeHuman Prescription Drug
Proprietary NamePantoprazole
Generic NamePantoprazole
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2011-01-19
Marketing CategoryANDA /
Application NumberANDA077619
Labeler NameNuCare Pharmaceuticals,Inc.
Substance NamePANTOPRAZOLE SODIUM
Active Ingredient Strength20 mg/1
Pharm ClassesProton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 68071-2891-6

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2891-6)
Marketing Start Date2022-11-30
NDC Exclude FlagN
Sample Package?N

Drug Details

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
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.