← FDA Drug Approvals (Drugs@FDA)
POTASSIUM CHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: YICHANG HUMANWELL · Approved 2018-06-22
Drug application
- FDA Application #
ANDA209314- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- POTASSIUM CHLORIDE
- Generic name
- POTASSIUM CHLORIDE
- Active ingredients
- POTASSIUM CHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- YICHANG HUMANWELL
- Manufacturer
- Slate Run Pharmaceuticals, LLC
- First approval
- 2018-06-22
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown