HEB Allergy Relief (cetirizine hydrochloride) NDC 37808-102

Product information

Brand name (proprietary)

HEB Allergy ReliefSuffix: Allergy Relief

Generic name (nonproprietary)

cetirizine hydrochloride

Active ingredients

Cetirizine hydrochloride — 5 mg/5mL

Dosage form

Solution

Route

Oral

Labeler

H E B

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, 2027

Other FDA classes

Histamine H1 Receptor Antagonists (Mechanism)

Identifiers

Product ID 37808-102_53296254-e9a0-3be3-e063-6394a90a742cSPL ID 53296254-e9a0-3be3-e063-6394a90a742cSPL set ID 9abdae64-4c3d-47f3-8224-fc81f7bfe557RxCUI 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

N437808010208 followed by a unit qualifier and the quantity Copy

Package 37808-0102-08. 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 090182

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