61919-700 : Pantoprazole Sodium D/R D/R 40 mg Oral Tablet, Delayed Release


NDC: 61919-700
Labeler: Direct Rx
Product Type: Human Prescription Drug
Drug Name:  Pantoprazole Sodium D/R
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA090074
Rev. Date: 


Appearance:


Markings: 97
Shapes:  Oval
Colors:  White
Size (mm): 11
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.

97: (13668-429) Pantoprazole Sodium D/R D/R 40 mg Oral Tablet, Delayed Release by Direct Rx
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:

  • 61919-700-30: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (61919‑700‑30)
  • 61919-700-40: 40 TABLET, DELAYED RELEASE IN 1 BOTTLE (61919‑700‑40)
  • 61919-700-90: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (61919‑700‑90)

Active Ingredients:

  • Pantoprazole Sodium

Dosage Strength:

  • 40 mg

Inactive Ingredients:

  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Propylene Glycol
  • Triethyl Citrate
  • Crospovidone
  • Hypromellose 2910 (3 Mpa.s)
  • Hydroxypropyl Cellulose (1600000 Wamw)
  • Mannitol
  • Calcium Stearate
  • Sodium Carbonate Decahydrate
  • Talc
  • Titanium Dioxide /
  • Propylene Glycol
  • Mannitol
  • Hypromellose 2910 (3 Mpa.s)
  • Talc
  • Triethyl Citrate
  • Hydroxypropyl Cellulose (1600000 Wamw)
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Sodium Carbonate Decahydrate
  • Titanium Dioxide
  • Calcium Stearate
  • Crospovidone /
  • Talc
  • Titanium Dioxide
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Sodium Carbonate Decahydrate
  • Hydroxypropyl Cellulose (1600000 Wamw)
  • Propylene Glycol
  • Crospovidone
  • Hypromellose 2910 (3 Mpa.s)
  • Triethyl Citrate
  • Calcium Stearate
  • Mannitol /

Pharmaceutical Classes:

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

NDC QR Code

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NDC 61919-700 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.