| NDC Code | 73473-902-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE (73473-902-10) |
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| Product NDC | 73473-902 |
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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 | 20250610 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216760 |
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| Manufacturer | Solaris Pharma Corporation |
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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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