NDC 70332-102
CYCLOPHENE
Cyclophene
CYCLOPHENE is a Kit in the Human Prescription Drug category. It is labeled and distributed by California Pharmaceuticals Llc. The primary component is .
| Product ID | 70332-102_99221323-f45d-4d12-abe4-0114ea75c187 |
| NDC | 70332-102 |
| Product Type | Human Prescription Drug |
| Proprietary Name | CYCLOPHENE |
| Generic Name | Cyclophene |
| Dosage Form | Kit |
| Marketing Start Date | 2016-01-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | California Pharmaceuticals LLC |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 70332-102-01
1 KIT in 1 KIT (70332-102-01) * 5.6 g in 1 BOTTLE * 100 g in 1 JAR * 5.6 g in 1 BOTTLE
| Marketing Start Date | 2016-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 70332-102-01 [70332010201]
CYCLOPHENE KIT
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2016-01-01 |
| Inactivation Date | 2020-01-31 |
Drug Details
OpenFDA Data
| SPL SET ID: | 26533d10-58da-6752-e054-00144ff8d46c |
| Manufacturer |
Trademark Results [CYCLOPHENE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CYCLOPHENE 72335883 0911764 Dead/Expired |
CHEMTRUST INDUSTRIES CORPORATION 1969-08-21 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.