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Micronase
Micronase - 0009-0171-07 - (glyburide)
Drug Information of Micronase
| Product NDC: | 0009-0171 |
| Proprietary Name: | Micronase |
| Non Proprietary Name: | glyburide |
| Active Ingredient(s): | 5 mg/1 & nbsp; glyburide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Micronase
| Product NDC: | 0009-0171 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017498 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19840501 |
Package Information of Micronase
| Package NDC: | 0009-0171-07 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0009-0171-07) |
NDC Information of Micronase
| NDC Code | 0009-0171-07 |
| Proprietary Name | Micronase |
| Package Description | 1000 TABLET in 1 BOTTLE (0009-0171-07) |
| Product NDC | 0009-0171 |
| 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 | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
