methylphenidate hydrochloride
- Product NDC
- 68084-816
- 11-digit product format
- 680840816
- Labeler code
- 68084
- Product ID
- 68084-816_951f9025-3dc9-8e0b-e053-2a95a90ac51a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA021121
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-08-21
- Marketing end
- 2020-08-31
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 27 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record