| NDC Code | 82432-101-01 |
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| Package Description | 1 VIAL, GLASS in 1 CARTON (82432-101-01) / 1 mL in 1 VIAL, GLASS |
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| Product NDC | 82432-101 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nalmefene Hydrochloride |
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| Non-Proprietary Name | Nalmefene Hydrochloride Injection |
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| Dosage Form | SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20231115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216007 |
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| Manufacturer | Chengdu Shuode Pharmaceutical Co., Ltd |
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| Substance Name | NALMEFENE HYDROCHLORIDE |
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| Strength | .1 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Opioid Antagonist [EPC], Opioid Antagonists [MoA] |
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