NDC Code | 70408-368-35 |
Package Description | 500 mL in 1 BOTTLE (70408-368-35) |
Product NDC | 70408-368 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylphenidate Hydrochloride |
Non-Proprietary Name | Methylphenidate Hydrochloride |
Dosage Form | SOLUTION |
Usage | ORAL |
Start Marketing Date | 20160106 |
Marketing Category Name | ANDA |
Application Number | ANDA201466 |
Manufacturer | Nostrum Laboratories, Inc. |
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 |