Cetirizine Hydrochloride (Allergy) NDC 71205-700

Product information

Brand name (proprietary)

Cetirizine Hydrochloride (Allergy)

Generic name (nonproprietary)

cetirizine hydrochloride

Active ingredients

Cetirizine hydrochloride — 10 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Proficient Rx LP

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090760

Marketing start

Aug 5, 2015

Listing expires

Dec 31, 2026

Other FDA classes

Histamine H1 Receptor Antagonists (Mechanism)

Identifiers

Product ID 71205-700_c5844e33-c337-4b62-91ca-de3d388b7d45SPL ID c5844e33-c337-4b62-91ca-de3d388b7d45SPL set ID d69083c4-b028-453c-8235-560b40ad358bRxCUI 1014678UNII 64O047KTOAUPC 0371205700102

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

N471205070000 followed by a unit qualifier and the quantity Copy

Package 71205-0700-00. 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 090760

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

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