| NDC Code | 17856-1927-2 |
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| Package Description | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1927-2) > 5 mL in 1 CUP, UNIT-DOSE |
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| Product NDC | 17856-1927 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Methadone Hydrocloride |
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| Proprietary Name Suffix | Dye-free, Sugar-free, Unflavored |
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| Non-Proprietary Name | Methadone Hydrochloride |
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| Dosage Form | CONCENTRATE |
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| Usage | ORAL |
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| Start Marketing Date | 20201102 |
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| End Marketing Date | 20220715 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212093 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | METHADONE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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