NDC 43386-070 - GaviLyte-H and Bisacodyl
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 43386-070
- Package NDCs from labels
- 43386-070-17
- Manufacturer
- Lupin Pharmaceuticals, Inc. | Novel Laboratories, Inc.
- Effective date
- 2025-01-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bisacodyl - Lupin Pharmaceuticals, Inc. | Novel Laboratories, Inc. | Lupin Pharmaceuticals, Inc. | Novel Laboratories, Inc. | 2025-01-28 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43386-070-17 | GaviLyte-H and Bisacodyl | 2 L in 1 BOTTLE | POWDER, FOR SOLUTION | 2 L | 5.6 g in 2L | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43386-070 | GAVILYTE-H AND BISACODYL (POLYETHYLENE GLYCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE AND BISACODYL DELAYED-RELEASE TABLET) KIT [LUPIN PHARMACEUTICALS, INC.] | 3 | Unmatched | 20250130_78fe1c29-e22a-4615-a2f9-a61cd4eb38a3.zip |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.