69367-305 : Miglitol 100 mg Oral Tablet, Coated


NDC69367-305
Labeler: Westminster Pharmaceuticals, LLC
Product Type: Human Prescription Drug
Drug Name:  Miglitol
Dosage Form: Oral Tablet, Coated
Application #: ANDA203965
Rev. Date: 


NDC Package Codes:

  • 69367-305-01: 100 TABLET, COATED IN 1 BOTTLE (69367‑305‑01)

Active Ingredients:

  • Miglitol

Dosage Strength:

  • 100 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 69367-303 Miglitol 25 mg Oral Tablet, Coated by Westminster Pharmaceuticals, LLC
  • 69367-304 Miglitol 50 mg Oral Tablet, Coated by Westminster Pharmaceuticals, LLC
  • 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.
  • 71205-935 Miglitol 25 mg Oral Tablet, Coated by Proficient Rx Lp
  • 71205-936 Miglitol 50 mg Oral Tablet, Coated by Proficient Rx Lp
  • 71205-937 Miglitol 100 mg Oral Tablet, Coated by Proficient Rx Lp
  • 76333-125 Miglitol 25 mg Oral Tablet, Coated by Orient Pharma Co., Ltd.
  • 76333-126 Miglitol 50 mg Oral Tablet, Coated by Orient Pharma Co., Ltd.
  • 76333-127 Miglitol 100 mg Oral Tablet, Coated by Orient Pharma Co., Ltd.

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