50090-5361 : Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release


NDC50090-5361
Labeler: A-s Medication Solutions
Product Type: Human Prescription Drug
Drug Name:  Pantoprazole Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA202038
Rev. Date: 


NDC Package Codes:

  • 50090-5361-0: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (50090‑5361‑0)
  • 50090-5361-1: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (50090‑5361‑1)
  • 50090-5361-2: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (50090‑5361‑2)

Active Ingredients:

  • Pantoprazole Sodium

Dosage Strength:

  • 20 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 50090-1100 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-1415 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-1416 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-1850 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-2275 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-2295 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-3095 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-4905 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-5378 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-5379 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-5793 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 50090-5794 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 54569-6062 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by A-s Medication Solutions
  • 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
  • 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.