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Daytrana
Daytrana - 68968-5555-3 - (methylphenidate)
Drug Information of Daytrana
| Product NDC: | 68968-5555 |
| Proprietary Name: | Daytrana |
| Non Proprietary Name: | methylphenidate |
| Active Ingredient(s): | 30 mg/9h & nbsp; methylphenidate |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Daytrana
| Product NDC: | 68968-5555 |
| Labeler Name: | Noven Therapeutics, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021514 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060406 |
Package Information of Daytrana
| Package NDC: | 68968-5555-3 |
| Package Description: | 30 PATCH in 1 CARTON (68968-5555-3) > 9 h in 1 PATCH |
NDC Information of Daytrana
| NDC Code | 68968-5555-3 |
| Proprietary Name | Daytrana |
| Package Description | 30 PATCH in 1 CARTON (68968-5555-3) > 9 h in 1 PATCH |
| Product NDC | 68968-5555 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylphenidate |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20060406 |
| Marketing Category Name | NDA |
| Labeler Name | Noven Therapeutics, LLC |
| Substance Name | METHYLPHENIDATE |
| Strength Number | 30 |
| Strength Unit | mg/9h |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
