| Product NDC: | 0054-3553 |
| 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: | 0054-3553 |
| Labeler Name: | Roxane Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089897 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880906 |
| Package NDC: | 0054-3553-44 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (0054-3553-44) |
| NDC Code | 0054-3553-44 |
| Proprietary Name | Methadone Hydrochloride |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (0054-3553-44) |
| Product NDC | 0054-3553 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methadone Hydrochloride |
| Dosage Form Name | CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 19880906 |
| 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] |