NDC 0008-0941

Protonix I.V.

Pantoprazole Sodium

Protonix I.V. is a Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is Pantoprazole Sodium.

• Product ID: 0008-0941_4770025a-60c9-492e-9d19-51ec395efef9
• NDC: 0008-0941
• Product Type: Human Prescription Drug
• Proprietary Name: Protonix I.V.
• Generic Name: Pantoprazole Sodium
• Dosage Form: Injection, Powder, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2001-05-01
• Marketing Category: NDA / NDA
• Application Number: NDA020988
• Labeler Name: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• Substance Name: PANTOPRAZOLE SODIUM
• Active Ingredient Strength: 40 mg/10mL
• Pharm Classes: Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0008-0941-03

25 CARTON in 1 PACKAGE (0008-0941-03) > 1 VIAL in 1 CARTON (0008-0941-01) > 10 mL in 1 VIAL

• Marketing Start Date: 2001-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0008-0941-03 [00008094103]

Protonix I.V. INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA020988
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2001-05-01

NDC 0008-0941-02 [00008094102]

Protonix I.V. INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA020988
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2001-05-01

NDC 0008-0941-01 [00008094101]

Protonix I.V. INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA020988
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2001-05-01

Drug Details

Active Ingredients

Ingredient	Strength
PANTOPRAZOLE SODIUM	40 mg/10mL

OpenFDA Data

• SPL SET ID: 48f4d638-d2a1-47fa-9a81-3acda1b1b1e3
• Manufacturer:
  • Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• UNII:
  • 6871619Q5X
• RxNorm Concept Unique ID - RxCUI:
  • 283669
  • 885257
• UPC Code:
  • 0300080941027
  • 0300080941010

Pharmacological Class

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

NDC Crossover Matching brand name "Protonix I.V." or generic name "Pantoprazole Sodium"

NDC	Brand Name	Generic Name
55154-4225	Protonix I.V.	Protonix I.V.
55154-4234	Protonix I.V.	Protonix I.V.
55154-4236	Protonix I.V.	Protonix I.V.
0093-0011	Pantoprazole Sodium	Pantoprazole Sodium
0093-0012	Pantoprazole Sodium	Pantoprazole Sodium
0143-9284	Pantoprazole Sodium	Pantoprazole Sodium
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