NDC codes

FDA NDC Directory
Product NDC (as listed)62332-502Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0502Add 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
62332-502-0362332050203623320502031 BOTTLE, PLASTIC in 1 CARTON (62332-502-03) / 2.5 mL in 1 BOTTLE, PLASTICMarketed from Apr 29, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 2 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
Alembic Pharmaceuticals Inc.NDC labeler code 62332
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209420
Marketing start
Listing expires
Other FDA classes
Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 62332-502_fb3ef8a7-46e3-4d8e-83df-117674d1c8aaSPL ID fb3ef8a7-46e3-4d8e-83df-117674d1c8aaSPL set ID dbcdf10c-5adb-4d48-97ce-f4b82c6bc77dRxCUI 1111343UNII 2XG66W44KFUPC 0362332502035
Pharmacologic class
Histamine-1 Receptor Inhibitor

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

N462332050203 followed by a unit qualifier and the quantity

Package 62332-0502-03. 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)

1 INDICATIONSAND USAGE Olopatadine hydrochloride ophthalmic solution USP, 0.2 % is indicated for the treatment of ocular itching associated with allergic conjunctivitis. Olopatadine hydrochloride ophthalmic solution USP, 0.2 % is a mast cell stabilizer indicated for the treatment of ocular itching associated with allergic conjunctivitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62332-502

What is NDC 62332-502?
62332-502 is the product NDC for Olopatadine Hydrochloride, Olopatadine hydrochloride 2 mg/mL solution/ drops, listed with the FDA by Alembic Pharmaceuticals Inc.. 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?
Alembic Pharmaceuticals Inc., NDC labeler code 62332. 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 209420

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

FDA NDC Directory listings under ANDA 209420
ProductStrengthForm · routeLabelerProduct NDC
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolution/ dropsOphthalmicAlembic Pharmaceuticals Limited46708-710
Olopatadine HydrochlorideOlopatadine hydrochloride 2 mg/mLSolution/ dropsOphthalmicAlembic Pharmaceuticals Inc.62332-710
Retaine Allergyolopatadine hydrochlorideOlopatadine hydrochloride 5 mg/2.5mLSolution/ dropsOphthalmicOCuSOFT LLC54799-920

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