| NDC Code | 79739-7183-1 |
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| Package Description | 100 TABLET in 1 BOTTLE (79739-7183-1) |
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| Product NDC | 79739-7183 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Mecamylamine Hydrochloride |
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| Non-Proprietary Name | Mecamylamine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20130319 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204054 |
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| Manufacturer | LGM PHARMA SOLUTIONS, LLC |
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| Substance Name | MECAMYLAMINE HYDROCHLORIDE |
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| Strength | 2.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Autonomic Ganglionic Blocker [EPC], Decreased Autonomic Ganglionic Activity [PE] |
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