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Picato
Picato - 50222-502-91 - (ingenol mebutate)
Drug Information of Picato
| Product NDC: | 50222-502 |
| Proprietary Name: | Picato |
| Non Proprietary Name: | ingenol mebutate |
| Active Ingredient(s): | 150 ug/g & nbsp; ingenol mebutate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Picato
| Product NDC: | 50222-502 |
| Labeler Name: | LEO Pharma Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202833 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120123 |
Package Information of Picato
| Package NDC: | 50222-502-91 |
| Package Description: | 3 TUBE in 1 CARTON (50222-502-91) > .47 g in 1 TUBE |
NDC Information of Picato
| NDC Code | 50222-502-91 |
| Proprietary Name | Picato |
| Package Description | 3 TUBE in 1 CARTON (50222-502-91) > .47 g in 1 TUBE |
| Product NDC | 50222-502 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ingenol mebutate |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120123 |
| Marketing Category Name | NDA |
| Labeler Name | LEO Pharma Inc. |
| Substance Name | INGENOL MEBUTATE |
| Strength Number | 150 |
| Strength Unit | ug/g |
| Pharmaceutical Classes | Cell Death Inducer [EPC],Increased Cellular Death [PE] |
