| NDC Code | 0378-4084-01 | 
|---|
			| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4084-01) | 
|---|
			| Product NDC | 0378-4084 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Dexmethylphenidate Hydrochloride | 
|---|
			
			| Non-Proprietary Name | Dexmethylphenidate Hydrochloride | 
|---|
			| Dosage Form | CAPSULE, EXTENDED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20131118 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA202580 | 
|---|
			| Manufacturer | Mylan Pharmaceuticals Inc. | 
|---|
			| Substance Name | DEXMETHYLPHENIDATE HYDROCHLORIDE | 
|---|
			| Strength | 30 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] | 
|---|
			| DEA Schedule | CII | 
|---|