| NDC Code | 10147-0685-1 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (10147-0685-1) |
|---|
| Product NDC | 10147-0685 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Methylphenidate Hydrochloride |
|---|
| Non-Proprietary Name | Methylphenidate Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20000801 |
|---|
| End Marketing Date | 20250531 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA021121 |
|---|
| Manufacturer | Patriot Pharmaceuticals, LLC. |
|---|
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
|---|
| Strength | 18 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE] |
|---|
| DEA Schedule | CII |
|---|