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Levatol
Levatol - 0091-4500-15 - (penbutolol sulfate)
Drug Information of Levatol
| Product NDC: | 0091-4500 |
| Proprietary Name: | Levatol |
| Non Proprietary Name: | penbutolol sulfate |
| Active Ingredient(s): | 20 mg/1 & nbsp; penbutolol sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levatol
| Product NDC: | 0091-4500 |
| Labeler Name: | UCB, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018976 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950615 |
Package Information of Levatol
| Package NDC: | 0091-4500-15 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0091-4500-15) |
NDC Information of Levatol
| NDC Code | 0091-4500-15 |
| Proprietary Name | Levatol |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0091-4500-15) |
| Product NDC | 0091-4500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | penbutolol sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19950615 |
| Marketing Category Name | NDA |
| Labeler Name | UCB, Inc. |
| Substance Name | PENBUTOLOL SULFATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
