Polyethylene Glycol 3350 NDC 72657-196

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

GLENMARK THERAPEUTICS INC., USA

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203928

Marketing start

Sep 19, 2024

Listing expires

Dec 31, 2027

Other FDA classes

Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)

Identifiers

Product ID 72657-196_7c2e19af-e03f-4d48-bac6-2efd716b70b3SPL ID 7c2e19af-e03f-4d48-bac6-2efd716b70b3SPL set ID 5aba6bb1-d25d-4901-8e9c-4cd4a3a06471RxCUI 876193UNII G2M7P15E5PUPC 0359556762079

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

N472657019616 followed by a unit qualifier and the quantity Copy

Package 72657-0196-16. 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

Other NDCs under ANDA 203928

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