52125-417 : Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet


NDC: 52125-417
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Pantoprazole Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA090797
Rev. Date: 


Appearance:


Markings: 40
Shapes:  Oval
Colors:  Yellow
Size (mm): 4
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 52125-417-19: 90 TABLET, DELAYED RELEASE IN 1 VIAL (52125‑417‑19)

Active Ingredients:

  • Pantoprazole Sodium

Dosage Strength:

  • 40 mg

Inactive Ingredients:

  • Ammonia
  • Sodium Lauryl Sulfate
  • Sodium Carbonate
  • Sodium Starch Glycolate Type a Potato
  • Shellac
  • Triethyl Citrate
  • Talc
  • Titanium Dioxide
  • Ferric Oxide Yellow
  • Calcium Stearate
  • Dimethylaminoethyl Methacrylate - Butyl Methacrylate - Methyl Methacrylate Copolymer
  • Ferrosoferric Oxide
  • Hypromelloses
  • Mannitol
  • Methacrylic Acid
  • Polyethylene Glycol 400
  • Propylene Glycol

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 52125-576 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Remedyrepack Inc.
  • 52125-838 Pantoprazole Sodium 20 mg/1 Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 52125-839 Pantoprazole Sodium 40 mg/1 Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 52125-916 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 52125-966 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 49349-809 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Remedyrepack Inc.
  • 49349-812 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Remedyrepack Inc.
  • 49349-851 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Remedyrepack Inc.
  • 49349-984 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Remedyrepack Inc.
  • 61786-118 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 61786-139 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 61786-200 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 61786-405 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 61786-427 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0012 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0226 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0286 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0395 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0860 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0962 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • More related products ...

NDC QR Code

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NDC 52125-417 QR Code

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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.