| NDC Code | 70069-431-05 |
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| Package Description | 5 VIAL in 1 CARTON (70069-431-05) / 2 mL in 1 VIAL (70069-431-01) |
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| Product NDC | 70069-431 |
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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 | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR |
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| Start Marketing Date | 20241105 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA214332 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | DICYCLOMINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
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