NDC Code | 70752-132-14 |
Package Description | 500 mL in 1 BOTTLE, PLASTIC (70752-132-14) |
Product NDC | 70752-132 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylphenidate Hydrochloride |
Non-Proprietary Name | Methylphenidate Hydrochloride |
Dosage Form | SOLUTION |
Usage | ORAL |
Start Marketing Date | 20200604 |
Marketing Category Name | ANDA |
Application Number | ANDA213567 |
Manufacturer | QUAGEN PHARMACEUTICALS LLC |
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 |