69367-305 : Miglitol 100 mg Oral Tablet, Coated
NDC: | 69367-305 |
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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