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: | 0406-8725-10 |
Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (0406-8725-10) |
NDC Code | 0406-8725-10 |
Proprietary Name | METHADOSE |
Package Description | 1000 mL in 1 BOTTLE, PLASTIC (0406-8725-10) |
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] |