Lidocaine Hydrochloride and Epinephrine
- Product NDC
- 70518-2062
- 11-digit product format
- 705182062
- Labeler code
- 70518
- Product ID
- 70518-2062_c5e8c5b7-2c6e-52e9-e053-2995a90a9079
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE and EPINEPHRINE
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA089644
- Marketing category
- ANDA
- Marketing start
- 2019-05-03
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE; EPINEPHRINE
- Active strength
- 10 mg/mL; ug/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE],Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-2062-0 | 70518206200 | 25 VIAL, MULTI-DOSE in 1 TRAY (70518-2062-0) > 20 mL in 1 VIAL, MULTI-DOSE | 2019-05-03 | 0000-00-00 | No | No | Current |