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Methadone Hydrochloride
Methadone Hydrochloride - 67457-217-20 - (Methadone Hydrochloride)
Drug Information of Methadone Hydrochloride
| Product NDC: | 67457-217 |
| Proprietary Name: | Methadone Hydrochloride |
| Non Proprietary Name: | Methadone Hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; Methadone Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methadone Hydrochloride
| Product NDC: | 67457-217 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021624 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19470813 |
Package Information of Methadone Hydrochloride
| Package NDC: | 67457-217-20 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (67457-217-20) > 20 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Methadone Hydrochloride
| NDC Code | 67457-217-20 |
| Proprietary Name | Methadone Hydrochloride |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (67457-217-20) > 20 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 67457-217 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methadone Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19470813 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | METHADONE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
