| NDC Code | 17856-0623-1 |
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| Package Description | 72 CUP, UNIT-DOSE in 1 PACKAGE (17856-0623-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0623-3) |
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| Product NDC | 17856-0623 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20200522 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212286 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | DICYCLOMINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
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