Vecamyl is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Vyera Pharmaceuticals, Llc. The primary component is Mecamylamine Hydrochloride.
Product ID | 69413-558_121b0c0e-01a4-4819-a777-2323af890f2a |
NDC | 69413-558 |
Product Type | Human Prescription Drug |
Proprietary Name | Vecamyl |
Generic Name | Mecamylamine Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2013-03-19 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA204054 |
Labeler Name | Vyera Pharmaceuticals, LLC |
Substance Name | MECAMYLAMINE HYDROCHLORIDE |
Active Ingredient Strength | 3 mg/1 |
Pharm Classes | Autonomic Ganglionic Blocker [EPC],Decreased Autonomic Ganglionic Activity [PE] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2013-03-19 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA204054 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-19 |
Ingredient | Strength |
---|---|
MECAMYLAMINE HYDROCHLORIDE | 2.5 mg/1 |
SPL SET ID: | 0774cc48-7287-4093-91d6-9df41a81408a |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
45043-558 | Vecamyl | Mecamylamine Hydrochloride |
69413-558 | Vecamyl | Mecamylamine Hydrochloride |
0722-7183 | Mecamylamine Hydrochloride | Mecamylamine Hydrochloride |
79739-7183 | Mecamylamine Hydrochloride | Mecamylamine Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VECAMYL 85278488 4358457 Live/Registered |
PHOENIXUS AG 2011-03-28 |