Fexofenadine hydrochloride NDC 55111-784

Product information

Brand name (proprietary)

Fexofenadine hydrochloride

Generic name (nonproprietary)

fexofenadine hydrochloride

Active ingredients

Fexofenadine hydrochloride — 180 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Dr. Reddy's Laboratories Limited

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 076502

Marketing start

Jan 3, 2011

Listing expires

Dec 31, 2027

Other FDA classes

Histamine H1 Receptor Antagonists (Mechanism)

Identifiers

Product ID 55111-784_c5d24cd6-8212-e647-78b1-27906e6f62bdSPL ID c5d24cd6-8212-e647-78b1-27906e6f62bdSPL set ID 864e3052-5787-bf11-9d17-11274ca2304fRxCUI 997420, 997488, 997501UNII 2S068B75ZU

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

N455111078401 followed by a unit qualifier and the quantity Copy

Package 55111-0784-01. 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 076502

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