Childrens Cetirizine Hydrochloride Sugar Free Grape NDC 51672-2102

Product information

Brand name (proprietary)

Childrens Cetirizine Hydrochloride Sugar Free GrapeSuffix: Sugar Free Grape

Generic name (nonproprietary)

cetirizine hydrochloride

Active ingredients

Cetirizine hydrochloride — 1 mg/mL

Dosage form

Solution

Route

Oral

Labeler

Sun Pharmaceutical Industries, Inc.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090182

Marketing start

Sep 8, 2011

Listing expires

Dec 31, 2026

Other FDA classes

Histamine H1 Receptor Antagonists (Mechanism)

Identifiers

Product ID 51672-2102_38f727a4-1153-9087-e063-6294a90ae97bSPL ID 38f727a4-1153-9087-e063-6294a90ae97bSPL set ID 54d72d7a-1f5b-4b36-bf76-ab7aef6243abRxCUI 1014673UNII 64O047KTOA

Pharmacologic class

Histamine-1 Receptor Antagonist

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

N451672210201 followed by a unit qualifier and the quantity Copy

Package 51672-2102-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 090182

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