NDC codes

FDA NDC Directory
Product NDC (as listed)70518-3232Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-3232Add 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
70518-3232-3705183232037051832320330 CAPSULE in 1 BLISTER PACK (70518-3232-3)Marketed from Mar 31, 2023
70518-3232-47051832320470518323204100 POUCH in 1 BOX (70518-3232-4) / 1 CAPSULE in 1 POUCH (70518-3232-5)Marketed from Dec 5, 2023
70518-3232-7705183232077051832320730 CAPSULE in 1 BLISTER PACK (70518-3232-7)Marketed from Jun 24, 2024

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 pamoate
Generic name (nonproprietary)
hydroxyzine pamoate
Active ingredients
Hydroxyzine pamoate — 50 mg/1
Dosage form
Capsule
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 086183
Marketing start
Listing expires
Other FDA classes
Histamine Receptor Antagonists (Mechanism)
Identifiers
Product ID 70518-3232_584f47c7-d3b9-2060-e063-6294a90a4d3aSPL ID 584f47c7-d3b9-2060-e063-6294a90a4d3aSPL set ID 0c9101ee-0746-4833-83cf-d0d09e52c0a9RxCUI 995278UNII M20215MUFR
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

N470518323203 followed by a unit qualifier and the quantity

Package 70518-3232-03. 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)

INDICATIONS 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 premedication and following general anesthesia, hydroxyzine may potentiate meperidine (Demerol ® ) 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 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-3232

What is NDC 70518-3232?
70518-3232 is the product NDC for Hydroxyzine pamoate, Hydroxyzine pamoate 50 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hydroxyzine pamoate.
What is the active ingredient?
Hydroxyzine pamoate.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. 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 pamoate?
81 other product NDCs are listed under this name. See all Hydroxyzine pamoate 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 pamoate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
hydroxyzine pamoateHydroxyzine pamoate 25 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-08787441-0087-01
hydroxyzine pamoateHydroxyzine pamoate 25 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-04087441-0040-01
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-04187441-0041-01
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-04287441-0042-01
hydroxyzine pamoateHydroxyzine pamoate 25 mg/1CapsuleOralCoupler LLC67046-028167046-0281-03
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralCoupler LLC67046-083167046-0831-03
hydroxyzine pamoateHydroxyzine pamoate 25 mg/1CapsuleOralCoupler LLC67046-208667046-2086-03
hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralREMEDYREPACK INC.70518-446370518-4463-0070518-4463-01
hydroxyzine pamoateHydroxyzine pamoate 25 mg/1CapsuleOralBryant Ranch Prepack72162-105472162-1054-03
hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-878968788-8789-03

All 82 Hydroxyzine pamoate NDCs

Other NDCs under ANDA 086183

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

FDA NDC Directory listings under ANDA 086183
ProductStrengthForm · routeLabelerProduct NDC
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralSandoz Inc0185-0676
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralA-S Medication Solutions50090-5933
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.66267-556
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralCoupler LLC67046-0831
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralBryant Ranch Prepack71335-2076
Hydroxyzine PamoateHydroxyzine pamoate 50 mg/1CapsuleOralDirect_Rx72189-480
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-041
Hydroxyzine pamoateHydroxyzine pamoate 50 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-042

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