Polyethylene Glycol 3350
- Product NDC
- 0722-6921
- 11-digit product format
- 007226921
- Labeler code
- 0722
- Product ID
- 0722-6921_d0d2f068-4453-4ea2-8282-339b6e497a9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Polyethylene Glycol 3350
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Nexgen Pharma, Inc.
- Application
- ANDA077706
- Marketing category
- ANDA
- Marketing start
- 2006-09-27
- Marketing end
- 0000-00-00
- Substance
- POLYETHYLENE GLYCOL 3350
- Active strength
- 17 g/1
- Pharmacologic classes
- Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0722-6921-01 | Polyethylene Glycol 3350 | 255 in 1 BOTTLE, PLASTIC | POWDER, FOR SOLUTION | 255 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0722-6921 | POLYETHYLENE GLYCOL 3350 POWDER, FOR SOLUTION [NEXGEN PHARMA, INC.] | 1 | Legacy NDC, 1 package rows | 20110825_d0d2f068-4453-4ea2-8282-339b6e497a9a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0722-6921-01 | 00722692101 | 255 in 1 BOTTLE, PLASTIC | Historical |