Lidocaine
- Product NDC
- 17478-811
- 11-digit product format
- 174780811
- Labeler code
- 17478
- Product ID
- 17478-811_f359d450-f447-447e-8f0d-9c9f58f14c2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- JELLY
- Route
- TOPICAL
- Labeler
- Akorn
- Application
- ANDA040433
- Marketing category
- ANDA
- Marketing start
- 2003-08-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-811-10 | 17478081110 | 1 TUBE in 1 CARTON (17478-811-10) > 5 mL in 1 TUBE | 1 tube | 2003-08-01 | 0000-00-00 | No | No | Current |
| 17478-811-30 | 17478081130 | 1 TUBE, WITH APPLICATOR in 1 CARTON (17478-811-30) > 30 mL in 1 TUBE, WITH APPLICATOR | | 2003-08-01 | 0000-00-00 | No | No | Current |