Imiquimod
- Product NDC
- 52549-4145
- 11-digit product format
- 525494145
- Labeler code
- 52549
- Product ID
- 52549-4145_2f2c5005-250a-452f-a8d2-05a505a0fb27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imiquimod
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Taro Pharmaceutical Industries Ltd.
- Application
- ANDA200173
- Marketing category
- ANDA
- Marketing start
- 2011-04-15
- Marketing end
- 0000-00-00
- Substance
- IMIQUIMOD
- Active strength
- 50 mg/g
- Pharmacologic classes
- Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52549-4145-6 | Imiquimod | 24 in 1 CARTON | CREAM | 24 | | 1 |
| 52549-4145-8 | Imiquimod | 0.25 g in 1 PACKET | CREAM | 0.25 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52549-4145 | IMIQUIMOD CREAM [TARO PHARMACEUTICAL INDUSTRIES LTD.] | 1 | Legacy NDC, 2 package rows | 20110714_47e471c2-4d26-4393-9f04-297fea8411ac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52549-4145-6 | 52549414506 | 24 in 1 CARTON | | Historical |
| 52549-4145-8 | 52549414508 | 0.25 g in 1 PACKET | 0.25 g | Historical |