POLYTHYLENE GLYCOL
- Product NDC
- 61919-879
- 11-digit product format
- 619190879
- Labeler code
- 61919
- Product ID
- 61919-879_9ab23521-8eec-5740-e053-2a95a90a1411
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POLYTHYLENE GLYCOL
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA090812
- Marketing category
- ANDA
- Marketing start
- 2019-07-30
- 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
- 2023-12-31
- 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 |
|---|
| 61919-879-51 | 61919087951 | 510 g in 1 BOTTLE (61919-879-51) | 510 g | 2019-07-30 | 0000-00-00 | No | No | Current |