Product NDC: | 0054-0391 |
Proprietary Name: | Methadone Hydrochloride |
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: | 0054-0391 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089897 |
Marketing Category: | ANDA |
Start Marketing Date: | 19880430 |
Package NDC: | 0054-0391-68 |
Package Description: | 1000 mL in 1 BOTTLE (0054-0391-68) |
NDC Code | 0054-0391-68 |
Proprietary Name | Methadone Hydrochloride |
Package Description | 1000 mL in 1 BOTTLE (0054-0391-68) |
Product NDC | 0054-0391 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Methadone Hydrochloride |
Dosage Form Name | CONCENTRATE |
Route Name | ORAL |
Start Marketing Date | 19880430 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | METHADONE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |