| NDC Code | 16571-259-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE (16571-259-10) |
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| Product NDC | 16571-259 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dicyclomine Hydrochloride |
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| Non-Proprietary Name | Dicyclomine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20241115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA218952 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | DICYCLOMINE HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
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