| NDC Code | 57664-368-35 |
|---|
| Package Description | 500 mL in 1 BOTTLE (57664-368-35) |
|---|
| Product NDC | 57664-368 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Methylphenidate Hydrochloride |
|---|
| Non-Proprietary Name | Methylphenidate Hydrochloride |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120301 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA201466 |
|---|
| Manufacturer | Caraco Pharmaceutical Laboratories, Ltd. |
|---|
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
|---|
| DEA Schedule | CII |
|---|