NDC 0527-1926
Methadone Hydrocloride
Methadone Hydrochloride
Methadone Hydrocloride is a Oral Concentrate in the Human Prescription Drug category. It is labeled and distributed by Lannett Company, Inc.. The primary component is Methadone Hydrochloride.
Product ID | 0527-1926_6714ab49-287c-460f-84c6-4a2eb909b896 |
NDC | 0527-1926 |
Product Type | Human Prescription Drug |
Proprietary Name | Methadone Hydrocloride |
Generic Name | Methadone Hydrochloride |
Dosage Form | Concentrate |
Route of Administration | ORAL |
Marketing Start Date | 2021-03-03 |
Marketing Category | ANDA / |
Application Number | ANDA212094 |
Labeler Name | Lannett Company, Inc. |
Substance Name | METHADONE HYDROCHLORIDE |
Active Ingredient Strength | 10 mg/mL |
Pharm Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |