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Glyset
Glyset - 0009-5012-01 - (MIGLITOL)
Drug Information of Glyset
| Product NDC: | 0009-5012 |
| Proprietary Name: | Glyset |
| Non Proprietary Name: | MIGLITOL |
| Active Ingredient(s): | 25 mg/1 & nbsp; MIGLITOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glyset
| Product NDC: | 0009-5012 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020682 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961218 |
Package Information of Glyset
| Package NDC: | 0009-5012-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0009-5012-01) |
NDC Information of Glyset
| NDC Code | 0009-5012-01 |
| Proprietary Name | Glyset |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0009-5012-01) |
| Product NDC | 0009-5012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MIGLITOL |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19961218 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | MIGLITOL |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC] |
