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Dexmethylphenidate Hydrochloride
Dexmethylphenidate Hydrochloride - 0093-5277-01 - (Dexmethylphenidate Hydrochloride)
Drug Information of Dexmethylphenidate Hydrochloride
| Product NDC: | 0093-5277 |
| Proprietary Name: | Dexmethylphenidate Hydrochloride |
| Non Proprietary Name: | Dexmethylphenidate Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Dexmethylphenidate Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dexmethylphenidate Hydrochloride
| Product NDC: | 0093-5277 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077107 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070608 |
Package Information of Dexmethylphenidate Hydrochloride
| Package NDC: | 0093-5277-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0093-5277-01) |
NDC Information of Dexmethylphenidate Hydrochloride
| NDC Code | 0093-5277-01 |
| Proprietary Name | Dexmethylphenidate Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (0093-5277-01) |
| Product NDC | 0093-5277 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dexmethylphenidate Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070608 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | DEXMETHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
