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Imiquimod
Imiquimod - 60505-0501-4 - (imiquimod)
Drug Information of Imiquimod
| Product NDC: | 60505-0501 |
| Proprietary Name: | Imiquimod |
| Non Proprietary Name: | imiquimod |
| Active Ingredient(s): | 50 mg/1000mg & nbsp; imiquimod |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Imiquimod
| Product NDC: | 60505-0501 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091308 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120914 |
Package Information of Imiquimod
| Package NDC: | 60505-0501-4 |
| Package Description: | 12 PACKET in 1 CARTON (60505-0501-4) > 250 mg in 1 PACKET |
NDC Information of Imiquimod
| NDC Code | 60505-0501-4 |
| Proprietary Name | Imiquimod |
| Package Description | 12 PACKET in 1 CARTON (60505-0501-4) > 250 mg in 1 PACKET |
| Product NDC | 60505-0501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | imiquimod |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120914 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | IMIQUIMOD |
| Strength Number | 50 |
| Strength Unit | mg/1000mg |
| Pharmaceutical Classes | Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA] |
