What is NDC 50844-772?

50844-772 is the product NDC for Polyethylene Glycol 3350, Polyethylene glycol 3350 17 g/17g powder, for solution, listed with the FDA by L.N.K. International, Inc.. It has 10 package NDCs, shown above in 10- and 11-digit form.

L.N.K. International, Inc., NDC labeler code 50844. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Polyethylene Glycol 3350?

28 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Polyethylene Glycol 3350 NDC 50844-772

NDC codes

FDA NDC Directory

Product NDC (as listed)50844-772Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50844-0772Add 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
50844-772-01	50844077201	30 PACKET in 1 CARTON (50844-772-01) / 17 g in 1 PACKETMarketed from Sep 10, 2026
50844-772-03	50844077203	10 PACKET in 1 CARTON (50844-772-03) / 17 g in 1 PACKETMarketed from Sep 10, 2026
50844-772-09	50844077209	20 PACKET in 1 CARTON (50844-772-09) / 17 g in 1 PACKETMarketed from Sep 10, 2026
50844-772-12	50844077212	100 PACKET in 1 CARTON (50844-772-12) / 17 g in 1 PACKETMarketed from Sep 10, 2026
50844-772-43	50844077243	17 g in 1 PACKET (50844-772-43)Marketed from Sep 10, 2026
50844-772-48	50844077248	14 PACKET in 1 CARTON (50844-772-48) / 17 g in 1 PACKETMarketed from Sep 10, 2026
50844-772-49	50844077249	238 g in 1 BOTTLE, PLASTIC (50844-772-49)Marketed from Sep 10, 2026
50844-772-90	50844077290	510 g in 1 BOTTLE, PLASTIC (50844-772-90)Marketed from Sep 10, 2026
50844-772-92	50844077292	119 g in 1 BOTTLE, PLASTIC (50844-772-92)Marketed from Sep 10, 2026
50844-772-93	50844077293	578 g in 1 BOTTLE, PLASTIC (50844-772-93)Marketed from Sep 10, 2026

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: L.N.K. International, Inc.NDC labeler code 50844
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217505
Marketing start: Sep 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 50844-772_41972e0f-61cb-43d5-a74e-f10ee85dcfe8SPL ID 41972e0f-61cb-43d5-a74e-f10ee85dcfe8SPL set ID bbc11078-73f7-4d27-b0d3-4d4ae5dae240RxCUI 876193UNII G2M7P15E5PUPC 0350844772039
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

N450844077201 followed by a unit qualifier and the quantity

Package 50844-0772-01. 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 Sep 10, 2026.

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)

About NDC 50844-772

What is NDC 50844-772?: 50844-772 is the product NDC for Polyethylene Glycol 3350, Polyethylene glycol 3350 17 g/17g powder, for solution, listed with the FDA by L.N.K. International, Inc.. It has 10 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Polyethylene Glycol 3350.
What is the active ingredient?: Polyethylene glycol 3350.
Who is the labeler?: L.N.K. International, Inc., NDC labeler code 50844. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Polyethylene Glycol 3350?: 28 other product NDCs are listed under this name. See all Polyethylene Glycol 3350 NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Polyethylene Glycol 3350 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	The Fresh Test, LLC	87362-119	87362-0119-01
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Aurobindo Pharma Limited	84386-125	84386-0125-0884386-0125-1484386-0125-24+1 more
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/1	Powder, For solutionOral	YYBA Corp	73581-913	73581-0913-40
Polyethylene Glycol 3350instalax polyethylene glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Sun Pharmaceutical Industries, Inc.	51672-2104	51672-2104-0351672-2104-0551672-2104-09
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Kesin Pharma Corporation	81033-762	81033-0762-0181033-0762-1481033-0762-30
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	NorthStar Rx LLC	72603-302	72603-0302-0272603-0302-0372603-0302-04
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	PIONEER LIFE SCIENCES, LLC	72090-036	72090-0036-0172090-0036-0272090-0036-03
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	CARDINAL HEALTH 110, LLC. DBA LEADER	70000-0699	70000-0699-02
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	GLENMARK THERAPEUTICS INC., USA	72657-196	72657-0196-16
Polyethylene Glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Preferred Pharmaceuticals Inc.	68788-8601	68788-8601-02

All 29 Polyethylene Glycol 3350 NDCs

Other NDCs under ANDA 217505

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

FDA NDC Directory listings under ANDA 217505
Product	Strength	Form · route	Labeler	Product NDC
Peg3350polyethylene glycol 3350	Polyethylene glycol 3350 17 g/17g	Powder, For solutionOral	Major Pharmaceuticals	0904-7534