LIDOCAINE HYDROCHLORIDE
- Product NDC
- 52584-095
- 11-digit product format
- 525840095
- Labeler code
- 52584
- Product ID
- 52584-095_14a92400-b26b-4707-9e26-6e028671bc09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA203082
- Marketing category
- ANDA
- Marketing start
- 2019-11-11
- Marketing end
- 2024-11-30
- 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
- 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 |
|---|
| 52584-095-05 | 52584009505 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-095-05) > 5 mL in 1 VIAL, SINGLE-DOSE | 2019-11-11 | 2024-11-30 | No | No | Current |