Prizotral
- Product NDC
- 59088-705
- 11-digit product format
- 590880705
- Labeler code
- 59088
- Product ID
- 59088-705_b45397b3-c77c-9fa0-e053-2995a90a56b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine and prilocaine, lidocaine hydrochloride
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-12-21
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 59088-705-00 | 59088070500 | 1 KIT in 1 PACKAGE (59088-705-00) * 1 TUBE in 1 CARTON (0591-2070-30) > 30 g in 1 TUBE * 1 TUBE in 1 CARTON (59088-371-07) > 85 g in 1 TUBE | 1 kit | 2017-12-21 | 0000-00-00 | No | No | Current |