← FDA Drug Approvals (Drugs@FDA)
DEXMETHYLPHENIDATE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: AUROLIFE PHARMA LLC · Approved 2013-08-28
Drug application
- FDA Application #
ANDA202580- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- DEXMETHYLPHENIDATE HYDROCHLORIDE
- Generic name
- Dexmethylphenidate Hydrochloride
- Active ingredients
- DEXMETHYLPHENIDATE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- AUROLIFE PHARMA LLC
- First approval
- 2013-08-28
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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