Lidothol
- Product NDC
- 68788-8129
- 11-digit product format
- 687888129
- Labeler code
- 68788
- Product ID
- 68788-8129_db7795f5-7131-4814-9ad7-3b5c583b6432
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HCl, MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-02-03
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE; MENTHOL, UNSPECIFIED FORM
- Active strength
- 5 g/100g; g/100g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8129 | LIDOTHOL (LIDOCAINE HCL, MENTHOL) GEL [PREFERRED PHARMACEUTICALS INC.] | 3 | Legacy NDC | 20240621_db7795f5-7131-4814-9ad7-3b5c583b6432.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8129-9 | 68788812909 | 1 TUBE in 1 BOX (68788-8129-9) > 99.2 g in 1 TUBE | 1 tube | 2022-02-03 | 0000-00-00 | No | No | Current |