| NDC Code | 50268-652-12 |
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| Package Description | 20 BLISTER PACK in 1 BOX (50268-652-12) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-652-11) |
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| Product NDC | 50268-652 |
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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 | 20210107 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077220 |
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| Manufacturer | AvPAK |
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| Substance Name | PILOCARPINE HYDROCHLORIDE |
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| Strength | 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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