Polyethylene Glycol 3350 NDC 68001-607

NDC codes

FDA NDC Directory

Product NDC (as listed)68001-607Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68001-0607Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
68001-607-55	68001060755	238 g in 1 BOTTLE (68001-607-55)Marketed from Oct 1, 2023
68001-607-69	68001060769	510 g in 1 BOTTLE (68001-607-69)Marketed from Oct 1, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Polyethylene Glycol 3350
Generic name (nonproprietary): polyethylene glycol 3350
Active ingredients: Polyethylene glycol 3350 — 17 g/17g
Dosage form: Powder, For solution
Route: Oral
Labeler: BluePoint Laboratories
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214990
Marketing start: Oct 1, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 68001-607_12fe5bcd-8ad0-e159-e063-6294a90a444eSPL ID 12fe5bcd-8ad0-e159-e063-6294a90a444eSPL set ID 02e36812-53c2-003b-e063-6394a90aed12RxCUI 876193UNII G2M7P15E5PUPC 0368001607551, 0368001607698
Pharmacologic class: Osmotic Laxative

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468001060755 followed by a unit qualifier and the quantity

Package 68001-0607-55. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 31, 2024.

Indications (excerpt from the label)

USE • relieves occasional constipation (irregularity) • generally produces a bowel movement in 1 to 3 days

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 214990

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 214990
Product	Strength	Form · route	Labeler	Product NDC
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Camber Consumer Care Inc	69230-324
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-002
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Preferred Pharmaceuticals Inc.	68788-8601
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/1	Powder, For solutionOral	YYBA Corp	73581-913
Polyethylene Gycol 3350	Polyethylene glycol 3350 17 g/g	Powder, For solutionOral	Allegiant Health	69168-473