Polyethylene Glycol 3350
- Product NDC
- 63629-2061
- 11-digit product format
- 636292061
- Labeler code
- 63629
- Product ID
- 63629-2061_e2b8d10f-9598-468a-85e9-be7a09dc36bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- polyethylene glycol 3350
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090812
- Marketing category
- ANDA
- Marketing start
- 2019-03-27
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 63629-2061-1 | 63629206101 | 238 g in 1 BOTTLE (63629-2061-1) | 238 g | 2021-02-09 | 0000-00-00 | No | No | Current |