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Methylin
Methylin - 59630-755-50 - (Methylphenidate Hydrochloride)
Drug Information of Methylin
| Product NDC: | 59630-755 |
| Proprietary Name: | Methylin |
| Non Proprietary Name: | Methylphenidate Hydrochloride |
| Active Ingredient(s): | 10 mg/5mL & nbsp; Methylphenidate Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylin
| Product NDC: | 59630-755 |
| Labeler Name: | SHIONOGI INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021419 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101101 |
Package Information of Methylin
| Package NDC: | 59630-755-50 |
| Package Description: | 500 mL in 1 BOTTLE (59630-755-50) |
NDC Information of Methylin
| NDC Code | 59630-755-50 |
| Proprietary Name | Methylin |
| Package Description | 500 mL in 1 BOTTLE (59630-755-50) |
| Product NDC | 59630-755 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylphenidate Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | NDA |
| Labeler Name | SHIONOGI INC. |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
