LIDOCAINE HYDROCHLORIDE
- Product NDC
- 68788-7999
- 11-digit product format
- 687887999
- Labeler code
- 68788
- Product ID
- 68788-7999_45eaf288-6e49-46a4-9f93-1beb5c9a2708
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA087872
- Marketing category
- ANDA
- Marketing start
- 2021-08-06
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- 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 |
|---|
| 68788-7999 | LIDOCAINE HYDROCHLORIDE SOLUTION [PREFERRED PHARMACEUTICALS INC.] | 4 | Legacy NDC | 20240621_5936d204-e171-4389-a207-718c02e5910c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7999-1 | 68788799901 | 100 mL in 1 BOTTLE, PLASTIC (68788-7999-1) | 100 ml | 2021-08-06 | 0000-00-00 | No | No | Current |