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Cetirizine Hydrochloride 10 mg Capsule, Liquid Filled, 12,000-count — NDC 61474-4370-1 (Billing 61474-4370-01)

by Catalent Ontario Limited · 12000 CAPSULE, LIQUID FILLED in 1 CARTON

This is a package of 12,000 capsules of Cetirizine Hydrochloride 10 mg Capsule, Liquid Filled from Catalent Ontario Limited, marketed since Aug 2023 and currently FDA-listed. It is this product's only package size.

NDC 61474-4370-01
🏷️ FDA NDC (as labeled) 61474-4370-1 billing pads the package segment with a zero
On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 61474-4370-1 alone.

Record
FDA NDC Directory package listing · Drug for further processing
Code segments
61474 labeler · 4370 product · 1 package
Package marketed since
Aug 17, 2023
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6147443701 4
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Cetirizine Hydrochloride (different manufacturers) — 3 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class I · Jun 24, 2026 — Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg. Determined to be Ranitidine. (JB Chemicals and Pharmaceuticals Ltd) · FDA recall D-0732-2026
Class III · Sep 12, 2025 — Tablet/Capsules Imprinted with Wrong ID (JB Chemicals and Pharmaceuticals Ltd) · FDA recall D-0032-2026
Class III · Sep 12, 2025 — Tablet/Capsules Imprinted with Wrong ID (JB Chemicals and Pharmaceuticals Ltd) · FDA recall D-0033-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61474-4370-1
Product NDC 61474-4370
11-digit billing NDC 61474437001
SPL Set ID 063555e9-f88a-7d22-e063-6294a90a2e3d
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-08-17
Dosage form CAPSULE, LIQUID FILLED
Substance CETIRIZINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 61474-4370-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 61474-4370-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It relieves allergy symptoms. Over-the-counter versions ease runny nose, sneezing, itchy, watery eyes and an itchy nose or throat from hay fever. Specific products treat hives, yea...
  • It can. Drowsiness was reported, and it was more common at higher doses in children. Be careful driving or using machinery until you know how it affects you, and avoid alcohol.
  • The oral solution can be taken with or without food. Food slightly delays how fast it works but does not change how much your body absorbs.
  • Check with me first if you take sedatives or tranquilizers, since they can add to drowsiness. The label found no significant interactions with azithromycin, pseudoephedrine, ketoco...
📖 Read our full Cetirizine guide →

Supplement & herbal interactions

Some supplements/herbs that may interact with Cetirizine Hydrochloride — tap one for details:

BeerModerate WineModerate Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Cetirizine Hydrochloride (5 interactions) — ranked by severity →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
61474-4370-01 You're viewing this Main listing 12000 CAPSULE, LIQUID FILLED in 1 CARTON — — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Sense All Day Allergy 10 mg 00113-0981-63 L. 25 capsules — — FDA listed —
Cetirizine Hydrochloride (Allergy) 10 mg 11822-4228-01 RITE 25 capsules — — FDA listed —
top care all day allergy 10 mg 36800-0180-09 Topco 65 capsules — — FDA listed —
24 hour allergy 10 mg 41250-0618-63 Meijer 25 capsules — — FDA listed —
CareOne Allergy Relief 10 mg 41520-0715-63 American 25 capsules — — FDA listed —
dg health all day allergy 10 mg 55910-0710-49 Dolgencorp, 40 capsules — — FDA listed —
dg health all day allergy 10 mg 55910-0934-49 Dolgencorp 40 capsules — — FDA listed —
allergy relief 10 mg 56062-0111-63 Publix 25 capsules — — FDA listed —
Cetirizine Hydrochloride (Allergy) 10 mg 58602-0716-16 Aurohealth 65 capsules — — FDA listed —
Cetirizine Hydrochloride (Hives Relief) 10 mg 58602-0808-04 Aurohealth 12 capsules — — FDA listed —
Cetirizine Hydrochloride (Allergy) 10 mg 58602-0863-12 Aurohealth 40 capsules — — FDA listed —
basic care all day allergy 10 mg 72288-0007-49 Amazon.com 40 capsules — — FDA listed —
Cetirizine Hydrochloride (Allergy) 10 mg 21130-0099-97 Better 25 capsules — — FDA listed —
topcare all day allergy 10 mg 36800-0448-09 Topco 65 capsules — — FDA listed —
careone allergy relief 10 mg 72476-0623-63 Retail 25 capsules — — FDA listed —
24 hour allergy 10 mg 79481-0981-00 Meijer, 25 capsules — — Discontinued —
Cetirizine Hydrochloride 10 mgthis 61474-4370-01 Catalent 12000 capsules — — FDA listed —
basic care all day allergy 10 mg 72288-0980-49 Amazon.com 40 capsules — — FDA listed —
Cetirizine Hydrochloride (Allergy) 10 mg 00363-0068-12 WALGREEN 40 capsules — — FDA listed —
Cetirizine Hydrochloride 10 mg 61474-4307-01 Catalent 12000 capsules — — FDA listed —
ZYRTEC Allergy 10 mg 50580-0786-12 Kenvue 12 capsules — — FDA listed —
Cetirizine Hydrochloride 10 mg 59651-0028-22 Aurobindo 2000 capsules — — FDA listed —
Cetirizine Hydrochloride 10 mg 59651-0027-22 Aurobindo 2000 capsules — — FDA listed —
Cetirizine Hydrochloride 10 mg 59651-0628-22 Aurobindo 2000 capsules — — FDA listed —
Cetirizine Hydrochloride (Allergy) 10 mg 58602-0806-04 Aurohealth 12 capsules — — FDA listed —
Zyrtec Allergy Cetirizine HCl 10 mg 67414-0012-00 Jones 90 capsules — — FDA listed —
cetirizine hydrochloride 10 mg 59556-0894-12 Strides 40 capsules — — FDA listed —
Amazon Basics All Day Allergy Relief 10 mg 72288-0013-40 Amazon.com 40 capsules — — FDA listed —
Zyrtec Allergy Cetirizine HCl 10 mg 67414-0013-01 Jones 12 capsules — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2023
On the market since
Aug 2023
📍
2026
Currently FDA-listed
3 years listed
🔒
·
Generic approved (availability unconfirmed)
see note
🔒Generic approved by FDA, but pharmacy availability is not confirmed

The FDA lists approved generic versions of this medicine, but that does not always mean a pharmacy can get one today. Patent rules, launch agreements, supply and pricing can affect when generics actually arrive.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

🧪 Avoiding an ingredient? See Cetirizine inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerCatalent Ontario Limited
Labeler code61474
First marketedAug 2023
Product typeDrug For Further Processing
Portfolio41 products on file

More NDCs from Catalent Ontario Limited labeler code 61474

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

Full FDA label FDA SPL

The complete FDA label for this product, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Listed for further processing / repackaging

What "drug for further processing" means

FDA lists this package under the "drug for further processing" marketing category: Catalent Ontario Limited supplies it to other companies for further processing or repackaging (blister cards that are later repackaged or co-packaged are a common example). The units themselves are a finished dosage form — which is why pricing or Medicaid data can still appear — but this exact package code may not be the presentation a retail pharmacy dispenses.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Drug For Further Processing". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Catalent Ontario Limited. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Catalent Ontario Limited is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 61474-4342-01 · Catalent 61474-4388-01 · Catalent →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.