NDC codes

FDA NDC Directory
Product NDC (as listed)0363-6340Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00363-6340Add 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
0363-6340-13003636340130036363401330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-6340-13)Marketed from Mar 20, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Hives Relief
Generic name (nonproprietary)
cetirizine tablets
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
WALGREEN COMPANYNDC labeler code 0363
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078862
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0363-6340_4d2c69cb-1f56-68a5-e063-6394a90a7074SPL ID 4d2c69cb-1f56-68a5-e063-6394a90a7074SPL set ID 4526b65c-b0e7-180c-e063-6394a90ae916RxCUI 1014678UNII 64O047KTOA
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

N400363634013 followed by a unit qualifier and the quantity

Package 00363-6340-13. 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)

Uses relieves itching due to hives (urticaria). This product will not prevent hives or an allergic skin reaction from occurring.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0363-6340

What is NDC 0363-6340?
0363-6340 is the product NDC for Hives Relief (cetirizine tablets), Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by WALGREEN COMPANY. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hives Relief (Cetirizine Tablets).
What is the active ingredient?
Cetirizine hydrochloride.
Who is the labeler?
WALGREEN COMPANY, NDC labeler code 0363. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hives Relief?
1 other product NDC are listed under this name. See all Hives Relief 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 Hives Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Hives Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1Tablet, Film coatedOralWalgreen Company0363-407100363-4071-39

Other NDCs under ANDA 078862

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

FDA NDC Directory listings under ANDA 078862
ProductStrengthForm · routeLabelerProduct NDC
Allergy Reliefcetirizine tabletsCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralDISCOUNT DRUG MART, INC53943-130
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralBionpharma Inc.69452-465

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