Tabradol is a Oral Kit in the Human Prescription Drug category. It is labeled and distributed by Fusion Pharmaceuticals Llc. The primary component is .
Product ID | 43093-101_28c7b9e3-07ca-6f9b-e054-00144ff88e88 |
NDC | 43093-101 |
Product Type | Human Prescription Drug |
Proprietary Name | Tabradol |
Generic Name | Cyclobenzaprine Hydrochloride |
Dosage Form | Kit |
Route of Administration | ORAL |
Marketing Start Date | 2009-09-17 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Fusion Pharmaceuticals LLC |
Active Ingredient Strength | 0 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2009-09-17 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2009-09-17 |
Inactivation Date | 2020-01-31 |
SPL SET ID: | 5d19ef8b-eef3-4d52-95f5-929765ca6dc7 |
Manufacturer |
NDC | Brand Name | Generic Name |
---|---|---|
70332-106 | Tabradol | Tabradol |
43093-101 | Tabradol | Tabradol |
0093-1920 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-1921 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-3420 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-3421 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-3422 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0115-1436 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0115-1437 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0179-0057 | cyclobenzaprine hydrochloride | cyclobenzaprine hydrochloride |
0179-0189 | cyclobenzaprine hydrochloride | cyclobenzaprine hydrochloride |
0378-0751 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0378-0761 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0378-0771 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0440-1350 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0440-7350 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0591-3256 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0591-3330 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0591-5658 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0615-3520 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0615-7528 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0615-8182 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0904-7809 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TABRADOL 85002366 3980334 Dead/Cancelled |
Fusion Pharmaceuticals 2010-03-30 |