NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1390Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1390Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
72162-1390-2721621390021 BOTTLE in 1 CARTON (72162-1390-2) / 240 SPRAY in 1 BOTTLEMarketed from Aug 29, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
olopatadine hydrochloride
Generic name (nonproprietary)
olopatadine hydrochloride
Active ingredients
Olopatadine hydrochloride — 665 ug/1
Dosage form
Spray
Route
Nasal
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202853
Marketing start
Listing expires
Other FDA classes
Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 72162-1390_1f877375-4665-4f9b-92af-93c6d73e2313SPL ID 1f877375-4665-4f9b-92af-93c6d73e2313SPL set ID db024b9c-681f-4503-9fda-1eaa1add4746RxCUI 1797895UNII 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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472162139002 followed by a unit qualifier and the quantity

Package 72162-1390-02. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Olopatadine hydrochloride nasal spray is indicated for the relief of the symptoms of seasonal allergic rhinitis in adults and pediatric patients 6 years of age and older. Olopatadine hydrochloride nasal spray is an H 1 receptor antagonist indicated for the relief of the symptoms of seasonal allergic rhinitis in adults and pediatric patients 6 years of age and older ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-1390

What is NDC 72162-1390?
72162-1390 is the product NDC for olopatadine hydrochloride, Olopatadine hydrochloride 665 ug/1 spray, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
olopatadine hydrochloride.
What is the active ingredient?
Olopatadine hydrochloride.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for olopatadine hydrochloride?
63 other product NDCs are listed under this name. See all olopatadine hydrochloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other olopatadine hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicYYBA CORP73581-71373581-0713-02
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicYYBA CORP73581-71273581-0712-02
Olopatadine Hydrochlorideolopatadine hydrochloride ophthalmicOlopatadine hydrochloride 1 mg/mLSolutionOphthalmicAmerisourceBergen Drug Corp46122-82346122-0823-29
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicAmerisourceBergen Drug Corp46122-82446122-0824-29
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicYYBA Corp73581-70973581-0709-02
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicWALGREEN COMPANY0363-086900363-0869-0100363-0869-02
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicBluePoint Laboratories68001-67468001-0674-92
Olopatadine HydrochlorideOlopatadine hydrochloride 1 mg/mLSolution/ dropsOphthalmicAllegiant Health69168-48069168-0480-0269168-0480-65
olopatadine hydrochlorideOlopatadine hydrochloride 2 mg/mLSolutionOphthalmicRising Pharma Holdings, Inc.16571-86116571-0861-25
olopatadine hydrochlorideOlopatadine hydrochloride 1 mg/mLSolutionOphthalmicRising Pharma Holdings, Inc.16571-88216571-0882-05

All 64 olopatadine hydrochloride NDCs

Other NDCs under ANDA 202853

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

FDA NDC Directory listings under ANDA 202853
ProductStrengthForm · routeLabelerProduct NDC
olopatadine hydrochlorideOlopatadine hydrochloride 665 ug/1SprayNasalPadagis Israel Pharmaceuticals Ltd45802-104
olopatadine hydrochlorideOlopatadine hydrochloride 665 ug/1SprayNasalBryant Ranch Prepack63629-8434

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