FDA NDC Directory · JSON-LD · Markdown
NDC 70436-002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Labeler / Manufacturer | Slate Run Pharmaceuticals, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA209314 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | POTASSIUM CHLORIDE (750 mg/1) |
| Marketing started | 20181115 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).