childrens allergy relief (loratadine) NDC 11822-0620

Product information

Brand name (proprietary)

childrens allergy relief

Generic name (nonproprietary)

loratadine

Active ingredients

Loratadine — 5 mg/5mL

Dosage form

Solution

Route

Oral

Labeler

Rite Aid Corporation

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075728

Marketing start

Apr 10, 2023

Marketing end

Dec 31, 2026

Identifiers

Product ID 11822-0620_845127a4-6d8b-44cb-9e25-b2393f147058SPL ID 845127a4-6d8b-44cb-9e25-b2393f147058SPL set ID 539336e6-7979-47ed-b1ea-fd46ef547aeeRxCUI 692783UNII 7AJO3BO7QN

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

N411822062000 followed by a unit qualifier and the quantity Copy

Package 11822-0620-00. 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 075728

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

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