FDA NDC Directory · JSON-LD · Markdown
NDC 43386-071 · HUMAN PRESCRIPTION DRUG · KIT
| Generic name | Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate, Potassium Chloride and Bisacodyl Delayed-release Tablet |
|---|---|
| Labeler / Manufacturer | Lupin Pharmaceuticals, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA202217 |
| Dosage form / route | KIT · ORAL |
| Active ingredients | — |
| Marketing started | 20150421 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).