LIDOCAINE
- Product NDC
- 71589-001
- 11-digit product format
- 715890001
- Labeler code
- 71589
- Product ID
- 71589-001_42e31939-85de-4fca-9bf6-c9ea88c29e2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA211469
- Marketing category
- ANDA
- Marketing start
- 2018-11-30
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 50 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- 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 |
|---|
| 71589-001-30 | 71589000130 | 1 TUBE in 1 CARTON (71589-001-30) > 30 g in 1 TUBE | 1 tube | 2018-11-30 | 0000-00-00 | No | No | Current |
| 71589-001-35 | 71589000135 | 1 TUBE in 1 CARTON (71589-001-35) > 35.44 g in 1 TUBE | 1 tube | 2018-11-30 | 0000-00-00 | No | No | Current |
| 71589-001-50 | 71589000150 | 50 g in 1 JAR (71589-001-50) | 50 g | 2018-11-30 | 0000-00-00 | No | No | Current |