Lidocaine Hydrochloride
- Product NDC
- 52584-277
- 11-digit product format
- 525840277
- Labeler code
- 52584
- Product ID
- 52584-277_3b9d1eb6-c435-4471-a1d8-c4fb08e43643
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride Anhydrous
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA088327
- Marketing category
- ANDA
- Marketing start
- 2010-09-01
- Marketing end
- 2024-03-01
- 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 |
|---|
| 52584-277-01 | 52584027701 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-277-01) > 20 mL in 1 VIAL, MULTI-DOSE | 2010-09-01 | 0000-00-00 | No | No | Current |
| 52584-277-02 | 52584027702 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-277-02) > 50 mL in 1 VIAL, MULTI-DOSE | 2010-09-01 | 2024-03-01 | No | No | Current |