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METHADOSE
METHADOSE - 0406-6974-34 - (methadone hydrochloride)
Drug Information of METHADOSE
| Product NDC: | 0406-6974 |
| Proprietary Name: | METHADOSE |
| 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) |
Labeler Information of METHADOSE
| Product NDC: | 0406-6974 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040050 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100223 |
Package Information of METHADOSE
| Package NDC: | 0406-6974-34 |
| Package Description: | 100 TABLET in 1 BOTTLE (0406-6974-34) |
NDC Information of METHADOSE
| NDC Code | 0406-6974-34 |
| Proprietary Name | METHADOSE |
| Package Description | 100 TABLET in 1 BOTTLE (0406-6974-34) |
| Product NDC | 0406-6974 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methadone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100223 |
| Marketing Category Name | ANDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | METHADONE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
