Product NDC: | 0054-8553 |
Proprietary Name: | METHADONE HYDROCHLORIDE |
Non Proprietary Name: | METHADONE HYDROCHLORIDE |
Active Ingredient(s): | 5 mg/1 & nbsp; METHADONE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-8553 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA006134 |
Marketing Category: | NDA |
Start Marketing Date: | 19470813 |
Package NDC: | 0054-8553-24 |
Package Description: | 4 BLISTER PACK in 1 CARTON (0054-8553-24) > 25 TABLET in 1 BLISTER PACK |
NDC Code | 0054-8553-24 |
Proprietary Name | METHADONE HYDROCHLORIDE |
Package Description | 4 BLISTER PACK in 1 CARTON (0054-8553-24) > 25 TABLET in 1 BLISTER PACK |
Product NDC | 0054-8553 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METHADONE HYDROCHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19470813 |
Marketing Category Name | NDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | METHADONE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |