Methylphenidate Hydrochloride (LA)
- Product NDC
- 51862-267
- 11-digit product format
- 518620267
- Labeler code
- 51862
- Product ID
- 51862-267_5a7c9051-b72d-4c35-9fd5-b670fc00e7f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mayne Pharma
- Application
- ANDA078458
- Marketing category
- ANDA
- Marketing start
- 2017-02-20
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record