| NDC Code | 63323-842-02 |
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| Package Description | 5 VIAL, SINGLE-DOSE in 1 CARTON (63323-842-02) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-842-21) |
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| Product NDC | 63323-842 |
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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 | 20190912 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210257 |
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| Manufacturer | Fresenius Kabi USA, 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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