FDA NDC Directory · JSON-LD · Markdown
NDC 71863-115 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION
| Labeler / Manufacturer | Eton Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA210508 |
| Dosage form / route | POWDER, FOR SOLUTION · ORAL |
| Active ingredients | BETAINE (1 g/g) |
| Marketing started | 20220128 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).