0480-4111 : Pantoprazole Sodium 40 mg/10ml Intravenous Injection, Powder, for Solution


NDC: 0480-4111
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Pantoprazole Sodium
Dosage Form: Intravenous Injection, Powder, for Solution
Application #: ANDA090296
Rev. Date: 


NDC Package Codes:

  • 0480-4111-03: 10 VIAL IN 1 CARTON (0480‑4111‑03) > 10 ML IN 1 VIAL (0480‑4111‑01)

Active Ingredients:

  • Pantoprazole Sodium

Dosage Strength:

  • 40 mg/10mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0008-0606 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
  • 0008-0607 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
  • 0093-0011 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Teva Pharmaceuticals USA Inc
  • 0093-0012 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Teva Pharmaceuticals USA Inc
  • 0143-9284 Pantoprazole Sodium 40 mg Intravenous Injection, Powder, Lyophilized, for Solution by West-ward Pharmaceuticals Corp
  • 0143-9300 Pantoprazole Sodium 40 mg Intravenous Injection, Powder, Lyophilized, for Solution by West-ward Pharmaceuticals Corp
  • 0338-9644 Pantoprazole Sodium 40 mg/100ml Intravenous Injection, Solution by Baxter Healthcare Corporation
  • 0338-9646 Pantoprazole Sodium 40 mg/50ml Intravenous Injection, Solution by Baxter Healthcare Corporation
  • 0338-9648 Pantoprazole Sodium 80 mg/100ml Intravenous Injection, Solution by Baxter Healthcare Corporation
  • 0378-6688 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Mylan Pharmaceuticals Inc.
  • 0378-6689 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Mylan Pharmaceuticals Inc.
  • 0615-7629 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-7916 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-7998 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-8113 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-8308 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0781-3232 Pantoprazole Sodium 40 mg/10ml Intravenous Injection, Powder, for Solution by Sandoz Inc
  • 0904-6474 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Major Pharmaceuticals
  • 0904-6870 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Major Pharmaceuticals
  • 13668-096 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Torrent Pharmaceuticals Limited
  • More related products ...

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.