NDC 0722-7183
Mecamylamine Hydrochloride
Mecamylamine Hydrochloride
Mecamylamine Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Nexgen Pharma, Inc.. The primary component is Mecamylamine Hydrochloride.
| Product ID | 0722-7183_9492a529-c29e-4833-9659-33b8a8694874 |
| NDC | 0722-7183 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Mecamylamine Hydrochloride |
| 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 | Nexgen Pharma, Inc. |
| 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 | 2020-12-31 |