NDC 59088-767
Cyclopak
Cyclobenzaprine Hydrochloride Tablet , Lidocaine And Prilocaine,
Cyclopak is a Kit in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is .
| Product ID | 59088-767_b56f8720-68be-16ed-e053-2995a90aac26 |
| NDC | 59088-767 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Cyclopak |
| Generic Name | Cyclobenzaprine Hydrochloride Tablet , Lidocaine And Prilocaine, |
| Dosage Form | Kit |
| Marketing Start Date | 2020-11-30 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | PureTek Corporation |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
Packaging
NDC 59088-767-00
1 KIT in 1 PACKAGE (59088-767-00) * 1 TUBE in 1 CARTON (0591-2070-30) > 30 g in 1 TUBE * 100 TABLET, FILM COATED in 1 BOTTLE (52817-330-10)
| Marketing Start Date | 2020-11-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
Drug Details
Trademark Results [Cyclopak]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CYCLOPAK 72207190 0813989 Dead/Expired |
BABCOCK & WILCOX COMPANY, THE 1964-12-01 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.