Lidocaine Hydrochloride and Dextrose
- Product NDC
- 0409-4712
- 11-digit product format
- 004094712
- Labeler code
- 0409
- Product ID
- 0409-4712_182e418c-9549-4815-8e91-76c85534f242
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride and dextrose
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRASPINAL
- Labeler
- Hospira, Inc.
- Application
- ANDA083914
- Marketing category
- ANDA
- Marketing start
- 2005-06-22
- Marketing end
- 0000-00-00
- Substance
- DEXTROSE MONOHYDRATE; LIDOCAINE HYDROCHLORIDE
- Active strength
- 75 mg/mL; 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 |
|---|
| 0409-4712-01 | 00409471201 | 5 CELLO PACK in 1 PACKAGE (0409-4712-01) > 5 AMPULE in 1 CELLO PACK (0409-4712-25) > 2 mL in 1 AMPULE (0409-4712-11) | 5 cello pack | 2005-06-22 | 0000-00-00 | No | No | Current |