CARTICEL is a Intra-articular Implant in the Human Prescription Drug category. It is labeled and distributed by Vericel Corporation. The primary component is Autologous Cultured Chondrocytes.
| Product ID | 69866-1025_45501f23-533e-4c7a-9203-2974d40c8a26 |
| NDC | 69866-1025 |
| Product Type | Human Prescription Drug |
| Proprietary Name | CARTICEL |
| Generic Name | Autologous Cultured Chondrocytes |
| Dosage Form | Implant |
| Route of Administration | INTRA-ARTICULAR |
| Marketing Start Date | 1905-06-19 |
| Marketing Category | BLA / BLA |
| Application Number | BLA103661 |
| Labeler Name | Vericel Corporation |
| Substance Name | AUTOLOGOUS CULTURED CHONDROCYTES |
| Active Ingredient Strength | 12000000 1/1 |
| Pharm Classes | Autologous Cultured Cell [EPC],Cells, Cultured, Autologous [EXT],Chondrocytes [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2015-11-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA103661 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-11-17 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| AUTOLOGOUS CULTURED CHONDROCYTES | 12000000 1/1 |
| SPL SET ID: | 096cf052-6510-412a-abf3-24e5a33ea316 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 69866-1025 | CARTICEL | autologous cultured chondrocytes |
| 69866-1030 | MACI | autologous cultured chondrocytes |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CARTICEL 75243080 2185013 Live/Registered |
VERICEL CORPORATION 1997-02-18 |
![]() CARTICEL 74732030 1998289 Live/Registered |
VERICEL CORPORATION 1995-09-15 |