| NDC Code | 16714-122-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (16714-122-01) |
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| Product NDC | 16714-122 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pilocarpine Hydrochloride |
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| Non-Proprietary Name | Pilocarpine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20190813 |
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| End Marketing Date | 20250831 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212377 |
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| Manufacturer | NorthStar Rx LLC |
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| Substance Name | PILOCARPINE HYDROCHLORIDE |
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| Strength | 7.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cholinergic Agonists [MoA], Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC] |
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