Vecamyl is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Manchester Pharmaceuticals. The primary component is Mecamylamine Hydrochloride.
| Product ID | 45043-558_976f404f-4857-4bad-9a3c-9bf3d5ca9f5b |
| NDC | 45043-558 |
| 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 | Manchester Pharmaceuticals |
| Substance Name | MECAMYLAMINE HYDROCHLORIDE |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Autonomic Ganglionic Blocker [EPC],Decreased Autonomic Ganglionic Activity [PE] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| 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 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| MECAMYLAMINE HYDROCHLORIDE | 2.5 mg/1 |
| SPL SET ID: | c6822ce4-e741-4366-b72a-5f5146354f97 |
| 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 |