Miglitol is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries Ltd.. The primary component is Miglitol.
| Product ID | 57664-685_17a6135f-ebee-4943-a5bf-b35df3d1ca27 |
| NDC | 57664-685 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Miglitol |
| Generic Name | Miglitol |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-01-04 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203965 |
| Labeler Name | Sun Pharmaceutical Industries Ltd. |
| Substance Name | MIGLITOL |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2016-04-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA203965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-04-21 |
| Ingredient | Strength |
|---|---|
| MIGLITOL | 50 mg/1 |
| SPL SET ID: | d6cea949-5b05-4c8e-b37f-40e33659510c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 57664-684 | Miglitol | Miglitol |
| 57664-685 | Miglitol | Miglitol |
| 57664-686 | Miglitol | Miglitol |
| 69367-303 | Miglitol | Miglitol |
| 69367-304 | Miglitol | Miglitol |
| 69367-305 | Miglitol | Miglitol |
| 71205-935 | Miglitol | Miglitol |
| 71205-936 | Miglitol | Miglitol |
| 71205-937 | Miglitol | Miglitol |
| 76333-125 | Miglitol | Miglitol |
| 76333-126 | Miglitol | Miglitol |
| 76333-127 | Miglitol | Miglitol |
| 0009-5012 | Glyset | miglitol |
| 0009-5013 | Glyset | miglitol |
| 0009-5014 | Glyset | miglitol |