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Monoket
Monoket - 0091-3620-18 - (isosorbide mononitrate)
Drug Information of Monoket
| Product NDC: | 0091-3620 |
| Proprietary Name: | Monoket |
| Non Proprietary Name: | isosorbide mononitrate |
| Active Ingredient(s): | 20 mg/1 & nbsp; isosorbide mononitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Monoket
| Product NDC: | 0091-3620 |
| Labeler Name: | UCB, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020215 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930630 |
Package Information of Monoket
| Package NDC: | 0091-3620-18 |
| Package Description: | 180 TABLET in 1 BOTTLE (0091-3620-18) |
NDC Information of Monoket
| NDC Code | 0091-3620-18 |
| Proprietary Name | Monoket |
| Package Description | 180 TABLET in 1 BOTTLE (0091-3620-18) |
| Product NDC | 0091-3620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | isosorbide mononitrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19930630 |
| Marketing Category Name | NDA |
| Labeler Name | UCB, Inc. |
| Substance Name | ISOSORBIDE MONONITRATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
