Product NDC: | 0009-0141 |
Proprietary Name: | Micronase |
Non Proprietary Name: | glyburide |
Active Ingredient(s): | 2.5 mg/1 & nbsp; glyburide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-0141 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017498 |
Marketing Category: | NDA |
Start Marketing Date: | 19840501 |
Package NDC: | 0009-0141-02 |
Package Description: | 100 TABLET in 1 BLISTER PACK (0009-0141-02) |
NDC Code | 0009-0141-02 |
Proprietary Name | Micronase |
Package Description | 100 TABLET in 1 BLISTER PACK (0009-0141-02) |
Product NDC | 0009-0141 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | glyburide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19840501 |
Marketing Category Name | NDA |
Labeler Name | Pharmacia and Upjohn Company |
Substance Name | GLYBURIDE |
Strength Number | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |