Olopatadine Hydrochloride NDC 79903-000

Product information

Brand name (proprietary)

Olopatadine Hydrochloride

Generic name (nonproprietary)

olopatadine hydrochloride

Active ingredients

Olopatadine hydrochloride — 1 mg/mL

Dosage form

Solution

Route

Ophthalmic

Labeler

Wal-Mart Stores, Inc.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 204812

Marketing start

Jul 15, 2020

Listing expires

Dec 31, 2026

Other FDA classes

Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)

Identifiers

Product ID 79903-000_2517db24-3263-45e7-aed0-7d955d198c96SPL ID 2517db24-3263-45e7-aed0-7d955d198c96SPL set ID 06467360-22fe-4a48-b234-06dbff30e853RxCUI 1111339UNII 2XG66W44KF

Pharmacologic class

Histamine-1 Receptor Antagonist; Histamine-1 Receptor Inhibitor; Mast Cell Stabilizer

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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N479903000040 followed by a unit qualifier and the quantity Copy

Package 79903-0000-40. 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 204812

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