Imiquimod is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Oceanside Pharmacueticals. The primary component is Imiquimod.
| Product ID | 68682-272_a97d5ae0-1ef7-4b0c-94e5-1f0ce9cb0fba |
| NDC | 68682-272 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Imiquimod |
| Generic Name | Imiquimod |
| Dosage Form | Cream |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2018-06-27 |
| Marketing Category | NDA / NDA AUTHORIZED GENERIC |
| Application Number | NDA022483 |
| Labeler Name | Oceanside Pharmacueticals |
| Substance Name | IMIQUIMOD |
| Active Ingredient Strength | 38 mg/g |
| Pharm Classes | Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2018-06-27 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA022483 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2018-06-27 |
| Ingredient | Strength |
|---|---|
| IMIQUIMOD | 37.5 mg/g |
| SPL SET ID: | d86eeb0e-70e0-4c72-aaa3-37daa1d8611e |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0093-3133 | Imiquimod | imiquimod |
| 0168-0432 | imiquimod | imiquimod |
| 45802-368 | Imiquimod | Imiquimod |
| 51672-4145 | Imiquimod | Imiquimod |
| 51672-4174 | Imiquimod | Imiquimod |
| 52549-4145 | Imiquimod | Imiquimod |
| 63629-8818 | Imiquimod | imiquimod |
| 64380-773 | imiquimod | imiquimod |
| 68462-536 | Imiquimod | Imiquimod |
| 68682-272 | Imiquimod | imiquimod |
| 72189-084 | IMIQUIMOD | IMIQUIMOD |
| 99207-260 | Aldara | imiquimod |
| 99207-270 | Zyclara | imiquimod |
| 99207-271 | Zyclara | imiquimod |
| 99207-276 | Zyclara | imiquimod |