| NDC Code | 65162-231-03 |
|---|
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-231-03) |
|---|
| Product NDC | 65162-231 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Methylphenidate Hydrochloride |
|---|
| Non-Proprietary Name | Methylphenidate Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180202 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207515 |
|---|
| Manufacturer | Amneal 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 |
|---|