← FDA Drug Approvals (Drugs@FDA)
METHYLPHENIDATE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS INC · Approved 2020-08-19
Drug application
- FDA Application #
ANDA205135- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- METHYLPHENIDATE HYDROCHLORIDE
- Generic name
- METHYLPHENIDATE HYDROCHLORIDE
- Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- SUN PHARM INDS INC
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- First approval
- 2020-08-19
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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