Polyethylene Glycol 3350
- Product NDC
- 71205-011
- 11-digit product format
- 712050011
- Labeler code
- 71205
- Product ID
- 71205-011_93f38248-3bd7-4cb6-969c-86bb8ddad18b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Polyethylene Glycol 3350
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077706
- Marketing category
- ANDA
- Marketing start
- 2006-09-06
- Marketing end
- 2021-07-31
- Substance
- POLYETHYLENE GLYCOL 3350
- Active strength
- 17 g/17g
- Pharmacologic classes
- Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-011-25 | 71205001125 | 255 g in 1 BOTTLE (71205-011-25) | 255 g | 2018-04-02 | 2021-07-31 | No | No | Current |