Scandonest 2% L
- Product NDC
- 0362-1097
- 11-digit product format
- 003621097
- Labeler code
- 0362
- Product ID
- 0362-1097_49286564-42b5-461b-9671-35ac106165ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mepivacaine Hydrochloride and Levonordefrin
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- Septodont, Inc.
- Application
- ANDA088388
- Marketing category
- ANDA
- Marketing start
- 2017-12-18
- Marketing end
- 0000-00-00
- Substance
- LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE
- Active strength
- 0 mg/mL; mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0362-1097-80 | 00362109780 | 5 BLISTER PACK in 1 CARTON (0362-1097-80) > 10 CARTRIDGE in 1 BLISTER PACK > 1.7 mL in 1 CARTRIDGE | 5 blister pack | 2017-12-18 | 0000-00-00 | No | No | Current |