NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1121Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1121Add 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
71335-1121-17133511210130 TABLET, FILM COATED in 1 BOTTLE (71335-1121-1)Marketed from Mar 7, 2019
71335-1121-271335112102100 TABLET, FILM COATED in 1 BOTTLE (71335-1121-2)Marketed from Mar 7, 2019
71335-1121-37133511210320 TABLET, FILM COATED in 1 BOTTLE (71335-1121-3)Marketed from Mar 7, 2019
71335-1121-47133511210490 TABLET, FILM COATED in 1 BOTTLE (71335-1121-4)Marketed from Apr 2, 2024
71335-1121-57133511210515 TABLET, FILM COATED in 1 BOTTLE (71335-1121-5)Marketed from Mar 7, 2019
71335-1121-67133511210660 TABLET, FILM COATED in 1 BOTTLE (71335-1121-6)Marketed from Mar 7, 2019
71335-1121-771335112107120 TABLET, FILM COATED in 1 BOTTLE (71335-1121-7)Marketed from Mar 7, 2019
71335-1121-87133511210810 TABLET, FILM COATED in 1 BOTTLE (71335-1121-8)Marketed from Mar 7, 2019

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)
Hydroxyzine Hydrochloride
Generic name (nonproprietary)
hydroxyzine hydrochloride
Active ingredients
Hydroxyzine dihydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040600
Marketing start
Listing expires
Other FDA classes
Histamine Receptor Antagonists (Mechanism)
Identifiers
Product ID 71335-1121_cd25e2c5-25ff-46ae-80ef-b01300cd959dSPL ID cd25e2c5-25ff-46ae-80ef-b01300cd959dSPL set ID 1c7d31fb-5e3c-456e-be6c-a3baafe60c37RxCUI 995218, 995258UNII 76755771U3
Pharmacologic class
Antihistamine

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

N471335112101 followed by a unit qualifier and the quantity

Package 71335-1121-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE For symptomatic relief of anxiety and tension associated with psychoneurosis and as an adjunct in organic disease states in which anxiety is manifested. Useful in the management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses and in histamine-mediated pruritus. As a sedative when used as a premedication and following general anesthesia, hydroxyzine may potentiate meperidine and barbiturates, so their use in pre-anesthetic adjunctive therapy should be modified on an individual basis. Atropine and other belladonna alkaloids are not affected by the drug. Hydroxyzine is not known to interfere with the action of digitalis in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040600

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

FDA NDC Directory listings under ANDA 040600
ProductStrengthForm · routeLabelerProduct NDC
Hydroxyzine HydrochlorideHydroxyzine hydrochloride 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8716
Hydroxyzine HydrochlorideHydroxyzine dihydrochloride 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1332

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