FDA NDC Directory · JSON-LD · Markdown
NDC 17856-0831 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION
| Labeler / Manufacturer | ATLANTIC BIOLOGICALS CORP. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA090313 |
| Dosage form / route | POWDER, FOR SUSPENSION · ORAL RECTAL |
| Active ingredients | SODIUM POLYSTYRENE SULFONATE (4.1 meq/g) |
| Marketing started | 20170207 |
| Package count | 0 |
Source: openFDA. Public-domain (CC0).