FDA NDC Directory · JSON-LD · Markdown
NDC 72789-503 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | Potassium Chloride |
|---|---|
| Labeler / Manufacturer | PD-Rx Pharmaceuticals, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA215725 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | POTASSIUM CHLORIDE (750 mg/1) |
| Marketing started | 20220725 |
| Package count | 1 |
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