NDC product
Womens Gentle Laxative
NDC 46122-429 · Amerisource Bergen
Key facts
| Product NDC | 46122-429 |
|---|---|
| Proprietary name | Womens Gentle Laxative |
| Nonproprietary name | Bisacodyl |
| Substances | BISACODYL |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Labeler | Amerisource Bergen |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
| Marketing start | Apr 1, 2013 |
| Marketing end | Feb 29, 2028 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory