What is NDC 68071-2237?

68071-2237 is the product NDC for HydrOXYzine Hydrochloride, Hydroxyzine dihydrochloride 25 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for HydrOXYzine Hydrochloride?

194 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

HydrOXYzine Hydrochloride NDC 68071-2237

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-2237Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-2237Add 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 NDC	11-digit (billing)	Package
68071-2237-2	6807122370268071223702	20 TABLET in 1 BOTTLE (68071-2237-2)Marketed from Aug 13, 2020
68071-2237-3	6807122370368071223703	30 TABLET in 1 BOTTLE (68071-2237-3)Marketed from Aug 13, 2020
68071-2237-5	6807122370568071223705	15 TABLET in 1 BOTTLE (68071-2237-5)Marketed from Nov 20, 2025

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 — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040840
Marketing start: Nov 11, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Histamine Receptor Antagonists (Mechanism)
Identifiers: Product ID 68071-2237_440bf439-8d43-df89-e063-6294a90ab70bSPL ID 440bf439-8d43-df89-e063-6294a90ab70bSPL set ID acc99b8f-87f0-eb3a-e053-2995a90aaaedRxCUI 995258UNII 76755771U3UPC 0368071223736
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

N468071223702 followed by a unit qualifier and the quantity

Package 68071-2237-02. 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 Nov 20, 2025.

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 i…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-2237

What is NDC 68071-2237?: 68071-2237 is the product NDC for HydrOXYzine Hydrochloride, Hydroxyzine dihydrochloride 25 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: HydrOXYzine Hydrochloride.
What is the active ingredient?: Hydroxyzine dihydrochloride.
Who is the labeler?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for HydrOXYzine Hydrochloride?: 194 other product NDCs are listed under this name. See all HydrOXYzine 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 HydrOXYzine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hydroxyzine Hydrochloride	Hydroxyzine hydrochloride 10 mg/5mL	SolutionOral	Advagen Pharma Limited	72888-218	72888-0218-13
Hydroxyzine hydrochloride	Hydroxyzine hydrochloride 50 mg/1	TabletOral	Coupler LLC	67046-0566	67046-0566-03
Hydroxyzine hydrochloride	Hydroxyzine hydrochloride 10 mg/1	TabletOral	Coupler LLC	67046-0833	67046-0833-03
Hydroxyzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0590	80425-0590-0180425-0590-0280425-0590-03
Hydroxyzine hydrochloride	Hydroxyzine hydrochloride 50 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-039	87441-0039-01
Hydroxyzine Hydrochloride	Hydroxyzine hydrochloride 10 mg/5mL	SolutionOral	Saptalis Pharmaceuticals, LLC.	71656-090	71656-0090-16
Hydroxyzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1311	67046-1311-03
Hydroxyzine hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	Coupler LLC	67046-0713	67046-0713-03
Hydroxyzine Hydrochloride	Hydroxyzine dihydrochloride 10 mg/5mL	SolutionOral	ANI Pharmaceuticals, Inc.	70954-912	70954-0912-10
Hydroxyzine Hydrochloride	Hydroxyzine hydrochloride 25 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2148	55154-2148-00

All 195 HydrOXYzine Hydrochloride NDCs

Other NDCs under ANDA 040840

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

FDA NDC Directory listings under ANDA 040840
Product	Strength	Form · route	Labeler	Product NDC
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 10 mg/1	TabletOral	Northstar RxLLC	16714-081
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	Northstar RxLLC	16714-082
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 50 mg/1	TabletOral	Northstar RxLLC	16714-083
HydrOXYzine Hydrochloride	Hydroxyzine hydrochloride 50 mg/1	TabletOral	A-S Medication Solutions	50090-2614
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-6626
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-6628
HydrOXYzine Hydrochloride	Hydroxyzine hydrochloride 10 mg/1	TabletOral	A-S Medication Solutions	50090-6682
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-7582
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 50 mg/1	TabletOral	Redpharm Drug	67296-2224
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3450
HydrOXYzine Hydrochloride	Hydroxyzine hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4360
HydrOXYzine Hydrochloride	Hydroxyzine dihydrochloride 25 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-686