NDC Code | 29033-208-01 |
Package Description | 100 TABLET in 1 BOTTLE (29033-208-01) |
Product NDC | 29033-208 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylphenidate Hydrochloride |
Non-Proprietary Name | Methylphenidate Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20170303 |
Marketing Category Name | ANDA |
Application Number | ANDA207587 |
Manufacturer | Nostrum Laboratories, Inc. |
Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
Strength | 20 |
Strength Unit | mg/1 |
Pharmacy Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
DEA Schedule | CII |