Lidomark 2/5
- Product NDC
- 69263-852
- 11-digit product format
- 692630852
- Labeler code
- 69263
- Product ID
- 69263-852_cd3d9628-6ce8-36e0-e053-2a95a90a1265
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine
- Dosage form
- KIT
- Route
- EPIDURAL; INFILTRATION; INTRACAUDAL
- Labeler
- Oaklock, LLC
- Application
- ANDA084625
- Marketing category
- ANDA
- Marketing start
- 2020-07-17
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69263-852-01 | 69263085201 | 1 KIT in 1 CARTON (69263-852-01) * 5 mL in 1 VIAL, SINGLE-DOSE (0143-9594-01) | 1 kit | 2020-07-17 | 0000-00-00 | No | No | Current |