Lidocaine Hydrochloride
- Product NDC
- 63739-457
- 11-digit product format
- 637390457
- Labeler code
- 63739
- Product ID
- 63739-457_66293b2e-6706-4223-a0b6-106a48dd4521
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA040302
- Marketing category
- ANDA
- Marketing start
- 2005-12-09
- 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
- 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 |
|---|
| 63739-457-21 | 63739045721 | 5 SYRINGE, PLASTIC in 1 BOX (63739-457-21) > 5 mL in 1 SYRINGE, PLASTIC | 2005-12-09 | 0000-00-00 | No | No | Current |