Lidorex
- Product NDC
- 59088-475
- 11-digit product format
- 590880475
- Labeler code
- 59088
- Product ID
- 59088-475_f2051c68-cdd9-58b2-e053-2995a90a6b48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine HCl
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-10-25
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 28 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lidorex
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 28 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 2562183 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-475-07 | Lidorex | 100 g in 1 TUBE | GEL | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-475 | LIDOREX (LIDOCAINE HCL) GEL [PURETEK CORPORATION] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230112_cc9eeba3-695d-d14e-e053-2a95a90a5c03.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59088-475-07 | 59088047507 | 100 g in 1 TUBE (59088-475-07) | 100 g | 2021-10-25 | 0000-00-00 | No | No | Current |