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imiquimod
imiquimod - 0168-0432-24 - (imiquimod)
Drug Information of imiquimod
| Product NDC: | 0168-0432 |
| Proprietary Name: | imiquimod |
| Non Proprietary Name: | imiquimod |
| Active Ingredient(s): | 50 mg/g & nbsp; imiquimod |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of imiquimod
| Product NDC: | 0168-0432 |
| Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078548 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100225 |
Package Information of imiquimod
| Package NDC: | 0168-0432-24 |
| Package Description: | 24 PACKET in 1 BOX (0168-0432-24) > .25 g in 1 PACKET (0168-0432-27) |
NDC Information of imiquimod
| NDC Code | 0168-0432-24 |
| Proprietary Name | imiquimod |
| Package Description | 24 PACKET in 1 BOX (0168-0432-24) > .25 g in 1 PACKET (0168-0432-27) |
| Product NDC | 0168-0432 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | imiquimod |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100225 |
| Marketing Category Name | ANDA |
| Labeler Name | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Substance Name | IMIQUIMOD |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA] |
