← FDA Drug Approvals (Drugs@FDA)
TUXARIN ER
NDA · New Drug Application · Sponsor: MAINPOINTE · Approved 2015-06-22
Drug application
- FDA Application #
NDA206323
- Application type
- New Drug Application
- Brand name
- TUXARIN ER
- Generic name
- CODEINE PHOSPHATE AND CHLORPHENIRAMINE MALEATE
- Active ingredients
- CHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- MAINPOINTE
- Manufacturer
- Mainpointe Pharmaceuticals
- First approval
- 2015-06-22
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown