lidocaine
- Product NDC
- 71205-500
- 11-digit product format
- 712050500
- Labeler code
- 71205
- Product ID
- 71205-500_f894693b-14d8-4cd5-b9c6-67f3f16333dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206498
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 98PI200987 | LIDOCAINE | 137-58-6 | LIDOCAINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-500-44 | 71205050044 | 1 TUBE in 1 CARTON (71205-500-44) / 35.44 g in 1 TUBE | 1 tube | 2020-11-04 | No | No | Historical |
| 71205-500-50 | 71205050050 | 50 g in 1 JAR (71205-500-50) | 50 g | 2021-05-07 | No | No | Historical |
| 71205-500-52 | 71205050052 | 8 TUBE in 1 CARTON (71205-500-52) / 35.44 g in 1 TUBE | 8 tube | 2020-11-04 | No | No | Historical |