52125-576 : Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet


NDC: 52125-576
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Pantoprazole Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA077058
Rev. Date: 


Appearance:


Markings: 124
Shapes:  Round
Colors:  Yellow
Size (mm): 8
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.

124: (47335-580) Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Remedyrepack Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 52125-576-02: 30 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (52125‑576‑02)
  • 52125-576-19: 90 TABLET, DELAYED RELEASE IN 1 VIAL (52125‑576‑19)

Active Ingredients:

  • Pantoprazole Sodium

Dosage Strength:

  • 40 mg

Inactive Ingredients:

  • Ferric Oxide Yellow
  • Ferrosoferric Oxide
  • Shellac
  • Titanium Dioxide
  • Isopropyl Alcohol
  • Ammonia
  • Butyl Alcohol
  • Propylene Glycol
  • Triethyl Citrate
  • Mannitol
  • Anhydrous Lactose
  • Crospovidone
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Sodium Carbonate
  • Povidone
  • Calcium Stearate
  • Polyethylene Glycols
  • Hypromelloses
  • Talc

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 52125-417 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 52125-576 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.