67877-443 : Rabeprazole Sodium Rabeprazole Sodium 20 mg Oral Tablet, Delayed Release


NDC67877-443
Labeler: Ascend Laboratories, LLC
Product Type: Human Prescription Drug
Drug Name:  Rabeprazole Sodium Rabeprazole Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA208644
Rev. Date: 


Appearance:


Markings: 20
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.

NDC Package Codes:

  • 67877-443-30: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (67877‑443‑30)
  • 67877-443-38: 100 POUCH IN 1 CARTON (67877‑443‑38) > 1 BLISTER PACK IN 1 POUCH > 10 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (67877‑443‑33)
  • 67877-443-90: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (67877‑443‑90)

Active Ingredients:

  • Rabeprazole Sodium

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Mannitol
  • Crospovidone
  • Magnesium Oxide
  • Isopropyl Alcohol
  • Sodium Stearyl Fumarate
  • Magnesium Stearate
  • Ethylcelluloses
  • Hypromellose Phthalate (31% Phthalate, 170 Cst)
  • Carnauba Wax
  • Alcohol
  • Diacetylated Monoglycerides
  • Polyvinyl Alcohol
  • Talc
  • Titanium Dioxide
  • Polyethylene Glycol, Unspecified
  • Lecithin, Soybean
  • Ferric Oxide Yellow
  • Shellac
  • Ferrosoferric Oxide
  • Propylene Glycol
  • Butyl Alcohol
  • Ammonia
  • Hydroxypropyl Cellulose (1600000 Wamw) /

Pharmaceutical Classes:

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

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.