Imiquimod
- Strength
- 50 mg/g
- Form
- Cream
Glenmark Pharmaceuticals Inc., USA
Listed by Sun Pharmaceutical Industries, Inc.
| Dosage form | Cream |
|---|---|
| Route | Topical |
| Approval route | ANDA — approved generic |
| NDC code | 51672-4174 |
| FDA application | ANDA205971 |
| RxNorm concept | 967017 |
| Package sizes listed | 2 |
| Marketed since | January 2021 |
Same active ingredient, different manufacturer, strength or form. Products matching on both ingredient and strength are usually interchangeable — but confirm before switching, especially with modified-release forms.
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Information only, not medical advice. Nothing on this page indicates that a medication is safe or suitable for you. Speak to a prescriber or pharmacist before starting, stopping or switching any medicine.
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