Lidocaine hydrochloride
- Product NDC
- 71205-973
- 11-digit product format
- 712050973
- Labeler code
- 71205
- Product ID
- 71205-973_5b4b36dd-da60-47de-a2c1-517a52ab3549
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-08-19
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| V13007Z41A | LIDOCAINE HYDROCHLORIDE | 6108-05-0 | LIDOCAINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-973-01 | 71205097301 | 1 TUBE in 1 CARTON (71205-973-01) / 28.35 g in 1 TUBE | 1 tube | 2020-05-11 | No | No | Historical |
| 71205-973-03 | 71205097303 | 1 TUBE in 1 CARTON (71205-973-03) / 85 g in 1 TUBE | 1 tube | 2020-05-11 | No | No | Historical |