NDC product
PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride
NDC 10572-302 · Affordable Pharmaceuticals, LLC
Key facts
| Product NDC | 10572-302 |
|---|---|
| Proprietary name | PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Nonproprietary name | polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride |
| Substances | POLYETHYLENE GLYCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE |
| Dosage form | POWDER, FOR SOLUTION |
| Route | ORAL |
| Labeler | Affordable Pharmaceuticals, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA019797 |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] and 1 more |
| Marketing start | Feb 8, 2013 |
| Marketing end | Mar 31, 2029 |
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