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Methadone Hydrochloride
Methadone Hydrochloride - 66689-695-79 - (Methadone Hydrochloride)
Drug Information of Methadone Hydrochloride
| Product NDC: | 66689-695 |
| 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) |
Labeler Information of Methadone Hydrochloride
| Product NDC: | 66689-695 |
| Labeler Name: | VistaPharm Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040088 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111201 |
Package Information of Methadone Hydrochloride
| Package NDC: | 66689-695-79 |
| Package Description: | 1000 mL in 1 BOTTLE (66689-695-79) |
NDC Information of Methadone Hydrochloride
| NDC Code | 66689-695-79 |
| Proprietary Name | Methadone Hydrochloride |
| Package Description | 1000 mL in 1 BOTTLE (66689-695-79) |
| Product NDC | 66689-695 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methadone Hydrochloride |
| Dosage Form Name | CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | ANDA |
| Labeler Name | VistaPharm Inc |
| Substance Name | METHADONE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
