| NDC Code | 70121-1712-2 |
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| Package Description | 10 POUCH in 1 CARTON (70121-1712-2) / 1 BAG in 1 POUCH / 100 mL in 1 BAG |
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| Product NDC | 70121-1712 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexmedetomidine Hydrochloride |
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| Non-Proprietary Name | Dexmedetomidine Hydrochloride In Sodium Chloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20230519 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216604 |
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| Manufacturer | Amneal Pharmaceuticals LLC |
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| Substance Name | DEXMEDETOMIDINE HYDROCHLORIDE |
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| Strength | 4 |
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| Strength Unit | ug/mL |
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| Pharmacy Classes | Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC], General Anesthesia [PE] |
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