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Mecamylamine Hydrochloride
Mecamylamine Hydrochloride - 0722-7183-01 - (Mecamylamine Hydrochloride)
Drug Information of Mecamylamine Hydrochloride
| Product NDC: | 0722-7183 |
| Proprietary Name: | Mecamylamine Hydrochloride |
| Non Proprietary Name: | Mecamylamine Hydrochloride |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; Mecamylamine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mecamylamine Hydrochloride
| Product NDC: | 0722-7183 |
| Labeler Name: | Nexgen Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA204054 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130319 |
Package Information of Mecamylamine Hydrochloride
| Package NDC: | 0722-7183-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0722-7183-01) |
NDC Information of Mecamylamine Hydrochloride
| NDC Code | 0722-7183-01 |
| Proprietary Name | Mecamylamine Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (0722-7183-01) |
| Product NDC | 0722-7183 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mecamylamine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130319 |
| Marketing Category Name | ANDA |
| Labeler Name | Nexgen Pharma, Inc. |
| Substance Name | MECAMYLAMINE HYDROCHLORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Autonomic Ganglionic Blocker [EPC],Decreased Autonomic Ganglionic Activity [PE] |
