| Product NDC: | 0406-8725 |
| Proprietary Name: | METHADOSE |
| Non Proprietary Name: | methadone hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; methadone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0406-8725 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017116 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100310 |
| Package NDC: | 0406-8725-15 |
| Package Description: | 15000 mL in 1 BOTTLE, PLASTIC (0406-8725-15) |
| NDC Code | 0406-8725-15 |
| Proprietary Name | METHADOSE |
| Package Description | 15000 mL in 1 BOTTLE, PLASTIC (0406-8725-15) |
| Product NDC | 0406-8725 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methadone hydrochloride |
| Dosage Form Name | CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20100310 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | METHADONE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |