Methylphenidate Hydrochloride
- Product NDC
- 62559-791
- 11-digit product format
- 625590791
- Labeler code
- 62559
- Product ID
- 62559-791_31b21c03-9605-4cee-88f8-0b9a813bc2ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA208607
- Marketing category
- ANDA
- Marketing start
- 2019-03-25
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record