LIDOCAINE HYDROCHLORIDE
- Product NDC
- 52584-279
- 11-digit product format
- 525840279
- Labeler code
- 52584
- Product ID
- 52584-279_c2bb3e6d-15da-4aaf-ab5f-1df8a04f41c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA088329
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Marketing end
- 2021-03-01
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-279-16 | 52584027916 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-279-16) > 30 mL in 1 VIAL, SINGLE-DOSE | 2018-07-02 | 2021-03-01 | No | No | Current |