Lidocaine Hydrochloride
- Product NDC
- 63739-469
- 11-digit product format
- 637390469
- Labeler code
- 63739
- Product ID
- 63739-469_8a5eff85-fec9-4a97-8fe4-aaf32e8eee13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA088299
- Marketing category
- ANDA
- Marketing start
- 2005-07-12
- 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
- 2021-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-469-21 | 63739046921 | 5 VIAL, MULTI-DOSE in 1 BOX (63739-469-21) > 50 mL in 1 VIAL, MULTI-DOSE | 2005-07-12 | 0000-00-00 | No | No | Current |