LIDOCAINE
- Product NDC
- 73240-004
- 11-digit product format
- 732400004
- Labeler code
- 73240
- Product ID
- 73240-004_dfc2121b-1cec-3e4f-e053-2995a90a1909
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LIDOCAINE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SUNFLORA, INC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-01-26
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 4 g/100g
- 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
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 |
|---|
| 73240-004-03 | 73240000403 | 85 g in 1 APPLICATOR (73240-004-03) | 85 g | 2021-01-26 | 0000-00-00 | No | No | Current |