Lucemyra is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Us Worldmeds, Llc. The primary component is Lofexidine Hydrochloride.
Product ID | 27505-050_2a5694e4-edac-4fc2-a9af-31dabd6b7c02 |
NDC | 27505-050 |
Product Type | Human Prescription Drug |
Proprietary Name | Lucemyra |
Generic Name | Lofexidine Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2018-06-18 |
Marketing Category | NDA / NDA |
Application Number | NDA209229 |
Labeler Name | US WorldMeds, LLC |
Substance Name | LOFEXIDINE HYDROCHLORIDE |
Active Ingredient Strength | 0 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2018-06-18 |
NDC Exclude Flag | N |
Sample Package? | Y |
Marketing Category | NDA |
Application Number | NDA209229 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-06-18 |
Marketing Category | NDA |
Application Number | NDA209229 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-06-18 |
Marketing Category | NDA |
Application Number | NDA209229 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-06-18 |
Ingredient | Strength |
---|---|
LOFEXIDINE HYDROCHLORIDE | .2 mg/1 |
SPL SET ID: | bdcfe803-b556-47db-a54f-ae0f0e5be016 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
27505-050 | Lucemyra | lofexidine hydrochloride |
78670-050 | Lucemyra | lofexidine hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LUCEMYRA 87980155 5753184 Live/Registered |
US WORLDMEDS, LLC 2016-04-26 |
LUCEMYRA 87980154 5753183 Live/Registered |
US WorldMeds, LLC 2016-10-31 |
LUCEMYRA 87220661 5915208 Live/Registered |
US WorldMeds, LLC 2016-10-31 |
LUCEMYRA 87014902 5845850 Live/Registered |
US WORLDMEDS, LLC 2016-04-26 |