LIDOCAINE HYDROCHLORIDE
- Product NDC
- 70518-3507
- 11-digit product format
- 705183507
- Labeler code
- 70518
- Product ID
- 70518-3507_e8044c6a-00ac-096c-e053-2995a90a766d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA087872
- Marketing category
- ANDA
- Marketing start
- 2022-09-02
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3507 | LIDOCAINE HYDROCHLORIDE SOLUTION [REMEDYREPACK INC.] | 2 | Legacy NDC | 20240116_0614801b-bbca-4adb-87e8-44f1165e2a2f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3507-0 | 70518350700 | 100 mL in 1 BOTTLE, PLASTIC (70518-3507-0) | 100 ml | 2022-09-02 | 0000-00-00 | No | No | Current |