| NDC Code: |
0781-5754 |
| Proprietary Name: |
Methylphenidate Hydrochloride |
| Suffix: |
SR |
| Non-Proprietary Name: |
methylphenidate hydrochloride |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
31-03-1982 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA018029 |
| Labeler: |
SANDOZ INC |
| Substance Name: |
METHYLPHENIDATE HYDROCHLORIDE |
| Active Numerator Strength: |
20 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
| DEA Schedule: |
CII |
