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DOLOPHINE
DOLOPHINE - 0054-4219-25 - (METHADONE HYDROCHLORIDE)
Drug Information of DOLOPHINE
| Product NDC: | 0054-4219 |
| Proprietary Name: | DOLOPHINE |
| Non Proprietary Name: | METHADONE HYDROCHLORIDE |
| Active Ingredient(s): | 10 mg/1 & nbsp; METHADONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOLOPHINE
| Product NDC: | 0054-4219 |
| Labeler Name: | Roxane Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA006134 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19470813 |
Package Information of DOLOPHINE
| Package NDC: | 0054-4219-25 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0054-4219-25) |
NDC Information of DOLOPHINE
| NDC Code | 0054-4219-25 |
| Proprietary Name | DOLOPHINE |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0054-4219-25) |
| Product NDC | 0054-4219 |
| 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 | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
