FDA NDC Directory · JSON-LD · Markdown
NDC 72657-196 · HUMAN OTC DRUG · POWDER, FOR SOLUTION
| Labeler / Manufacturer | GLENMARK THERAPEUTICS INC., USA |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA203928 |
| Dosage form / route | POWDER, FOR SOLUTION · ORAL |
| Active ingredients | POLYETHYLENE GLYCOL 3350 (17 g/17g) |
| Marketing started | 20240919 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).