FDA NDC Directory · JSON-LD · Markdown
NDC 62135-937 · HUMAN PRESCRIPTION DRUG · POWDER
| Labeler / Manufacturer | Chartwell RX, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA074562 |
| Dosage form / route | POWDER · ORAL |
| Active ingredients | CHOLESTYRAMINE (4 g/5.7g) |
| Marketing started | 19960815 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).