| NDC Code | 70436-147-81 |
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| Package Description | 5 VIAL, SINGLE-DOSE in 1 BOX (70436-147-81) / 2 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 70436-147 |
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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 |
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| Usage | INTRAMUSCULAR |
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| Start Marketing Date | 20210923 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207076 |
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| Manufacturer | Slate Run Pharmaceuticals, LLC |
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| Substance Name | DICYCLOMINE HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/2mL |
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| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
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