NDC Code | 68084-890-25 |
Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-890-25) > 1 TABLET in 1 BLISTER PACK (68084-890-95) |
Product NDC | 68084-890 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylphenidate Hydrochloride |
Non-Proprietary Name | Methylphenidate Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20150115 |
End Marketing Date | 20171031 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA021121 |
Manufacturer | American Health Packaging |
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 |