76333-126 : Miglitol 50 mg Oral Tablet, Coated


NDC76333-126
Labeler: Orient Pharma Co., Ltd.
Product Type: Human Prescription Drug
Drug Name:  Miglitol
Dosage Form: Oral Tablet, Coated
Application #: ANDA203965
Rev. Date: 


Appearance:


Markings: OP;26
Shapes:  Round
Colors:  White
Size (mm): 7
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:

  • 76333-126-11: 100 TABLET, COATED IN 1 BOTTLE (76333‑126‑11)
  • 76333-126-12: 1000 TABLET, COATED IN 1 BOTTLE (76333‑126‑12)

Active Ingredients:

  • Miglitol

Dosage Strength:

  • 50 mg

Inactive Ingredients:

  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Starch, Corn
  • Hypromelloses
  • Polyethylene Glycol 400
  • Titanium Dioxide
  • Polysorbate 80

Pharmaceutical Classes:

  • alpha Glucosidase Inhibitors [MoA]
  • alpha-Glucosidase Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
  • 76333-125 Miglitol 25 mg Oral Tablet, Coated by Orient Pharma Co., Ltd.
  • 76333-127 Miglitol 100 mg Oral Tablet, Coated by Orient Pharma Co., Ltd.
  • 57664-684 Miglitol 25 mg Oral Tablet, Coated by Sun Pharmaceutical Industries Ltd.
  • 57664-685 Miglitol 50 mg Oral Tablet, Coated by Sun Pharmaceutical Industries Ltd.
  • 57664-686 Miglitol 100 mg Oral Tablet, Coated by Sun Pharmaceutical Industries Ltd.

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