Amrix is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Lake Erie Medical Dba Quality Care Products Llc. The primary component is Cyclobenzaprine Hydrochloride.
Product ID | 35356-262_23bf2785-8ee7-4c37-a4d8-dc520b107602 |
NDC | 35356-262 |
Product Type | Human Prescription Drug |
Proprietary Name | Amrix |
Generic Name | Cyclobenzaprine Hydrochloride |
Dosage Form | Capsule, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2012-01-03 |
Marketing Category | NDA / NDA |
Application Number | NDA021777 |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Active Ingredient Strength | 15 mg/1 |
Pharm Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2012-01-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-01-03 |
Marketing End Date | 2019-10-11 |
Marketing Category | NDA |
Application Number | NDA021777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-01-03 |
Marketing End Date | 2017-01-01 |
Marketing Category | NDA |
Application Number | NDA021777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-01-03 |
Marketing End Date | 2017-01-01 |
Ingredient | Strength |
---|---|
CYCLOBENZAPRINE HYDROCHLORIDE | 15 mg/1 |
SPL SET ID: | 67c46f2e-59fe-4c20-a07d-79935d496d1f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
21695-723 | AMRIX | AMRIX |
21695-953 | AMRIX | AMRIX |
35356-262 | Amrix | Amrix |
50090-1101 | AMRIX | AMRIX |
63459-700 | AMRIX | AMRIX |
63459-701 | AMRIX | AMRIX |
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 |
---|---|
AMRIX 78261264 3353178 Live/Registered |
TEVA PHARMACEUTICALS INTERNATIONAL GMBH 2003-06-11 |
AMRIX 77307173 3684884 Live/Registered |
TEVA PHARMACEUTICALS INTERNATIONAL GMBH 2007-10-18 |