ReadySharp Lidocaine
- Product NDC
- 53225-3600
- 11-digit product format
- 532253600
- Labeler code
- 53225
- Product ID
- 53225-3600_cdc80d2f-c935-b2db-e053-2995a90a8759
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
- Labeler
- Terrain Pharmaceuticals
- Application
- ANDA203082
- Marketing category
- ANDA
- Marketing start
- 2013-03-14
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 53225-3600-1 | 53225360001 | 2 mL in 1 AMPULE (53225-3600-1) | 2 ml | 2016-11-14 | 0000-00-00 | No | No | Current |