Lidocaine Hydrochloride
- Product NDC
- 53002-3430
- 11-digit product format
- 530023430
- Labeler code
- 53002
- Product ID
- 53002-3430_ccb27e1b-23f0-4f90-a928-6cd5af3d9920
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL; TOPICAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA040014
- Marketing category
- ANDA
- Marketing start
- 1995-07-10
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-3430-1 | 53002343001 | 100 mL in 1 BOTTLE, PLASTIC (53002-3430-1) | 100 ml | 2018-10-01 | 0000-00-00 | No | No | Current |