55700-615 : Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release


NDC55700-615
Labeler: Lake Erie Medical Dba Quality Care Products LLC
Product Type: Human Prescription Drug
Drug Name:  Pantoprazole Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA090074
Rev. Date: 


Appearance:


Markings: 96
Shapes:  Oval
Colors:  White
Size (mm): 9
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.

96: (13668-096) Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Lake Erie Medical Dba Quality Care Products LLC
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:

  • 55700-615-30: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (55700‑615‑30)
  • 55700-615-60: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (55700‑615‑60)

Active Ingredients:

  • Pantoprazole Sodium

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Calcium Stearate
  • Crospovidone
  • Hydroxypropyl Cellulose (Type H)
  • Hypromellose 2910 (3 Mpa.s)
  • Mannitol
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Propylene Glycol
  • Sodium Carbonate
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 55700-019 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-062 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-314 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-318 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-329 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-790 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Quality Care Products, LLC
  • 55700-850 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Quality Care Products, LLC
  • 35356-622 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 35356-768 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Lake Erie Medical Dba Quality Care Products LLC
  • 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.
  • More related products ...

NDC 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.