Claritin-D 24 Hour Loratadine pseudoephedrine sulfate 10 mg; 240 mg Tablet, Extended Release, 10-count
by Bayer HealthCare LLC. · 1 BLISTER PACK in 1 CARTON (11523-0102-1) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
NDC 11523-0102-01
🏷️ FDA NDC (as labeled)
11523-0102-1
billing pads the package segment with a zero
This package
Contains10-count
Pack sizes2 compare ↓
Also comes in:
15 tablets 11523-0102-02
OTC
Generic
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
11523-0102-1
Product NDC
11523-0102
11-digit billing NDC
11523010201
UNII
7AJO3BO7QN, Y9DL7QPE6B
Application #
ANDA075706
SPL Set ID
3ea6a90b-8cb1-46b0-9ff7-be7090245e53
Established class (EPC)
alpha-Adrenergic Agonist
Mechanism of action
Adrenergic alpha-Agonists
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2022-12-12
Route
ORAL
Dosage form
TABLET, EXTENDED RELEASE
Substance
LORATADINE; PSEUDOEPHEDRINE SULFATE
GCN Seq No
027622
GCN
63577
HICL code
006605
Ingredient (HICL)
Loratadine/Pseudoephedrine
HIC1 code
Z
Therapeutic class — broad (HIC1)
Body As A Whole
HIC2 code
Z2
Therapeutic class — intermediate (HIC2)
Antihistamines, Antiserotonins, Immunosuppressants
HIC3 code
Z2O
Therapeutic class — specific (HIC3)
2Nd Gen Antihistamine And Decongestant Combination
AHFS code
04:08.00.00
AHFS class
Second Generation Antihistamines
FDB label name
CLARITIN-D 24 HOUR TABLET
FDB brand name
Claritin-D 24 Hour
Legend status
O — Over-the-counter (OTC) drug or device
Why two NDCs?
The FDA registers this code as 11523-0102-1 — 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 → 11523-0102-01. 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.
🏷️ RxNorm drug class
This medicine belongs to the Other antihistamines for systemic use class.
Drug family (ATC)
Other antihistamines for systemic use
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerBayer HealthCare LLC.
Application holderP AND L DEVELOPMENT LLC
FDA applicationANDA075706 (ANDA)
Labeler code11523
First marketedDec 2022
Product typeHuman Otc Drug
Portfolio240 products on file
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.
🩺 Clinical
Label name CLARITIN-D 24 HOUR TABLET Ingredient Loratadine/Pseudoephedrine
📗 Our plain-language guide HelloPharmacist
- Great question. The two ingredients each do something different. Loratadine is an antihistamine — it targets the sneezing, runny nose, itchy eyes, and throat itching that come with...
- What exactly does this medicine do, and why does it have two ingredients?
- You take it by mouth with a full glass of water — but it's really important that you swallow it whole. Do not crush, split, chew, or dissolve it. These are extended-release tablets...
- How do I take it, and does it matter if I crush or split the tablet?
Patient education
Supplement & herbal interactions
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.
💬 Questions about Loratadine pseudoephedrine sulfate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
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.
💲 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 system | Per each | Per 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.
Try another pack size:
15 tablets
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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| allergy d 10 mg/1; 240 mg 00113-9004-22 | L. | 1 tablet | $0.566 | — | Availability likely | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 00904-5833-15 | Major | 10 tablets | $0.566 | — | Availability likely | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 46122-0167-52 | Amerisource | 10 tablets | $0.566 | — | Availability likely | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 46122-0383-22 | AMERISOURCE | 15 tablets | $0.566 | — | Availability likely | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 51660-0724-04 | Ohm | 5 tablets | $0.566 | — | Availability likely | — |
| Leader Allergy Relief D-24 10 mg/1; 240 mg 70000-0162-01 | Cardinal | 10 tablets | $0.566 | — | Availability likely | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 70677-1018-01 | STRATEGIC | 10 tablets | $0.566 | — | Availability likely | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 49348-0543-01 | STRATEGIC | 10 tablets | $0.574 | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 62011-0071-01 | Strategic | 10 tablets | $0.574 | — | FDA listed | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 00363-0725-15 | Walgreen | 15 tablets | — | — | FDA listed | — |
| Allergy Relief D 10 mg/1; 240 mg 00363-2010-22 | Walgreen | 1 tablet | — | — | FDA listed | — |
| Claritin-D 24 Hour 10 mg/1; 240 mgthis 11523-0102-01 | Bayer | 10 tablets | — | — | FDA listed | — |
| Claritin-D 24 Hour 10 mg/1; 240 mg 11523-4332-01 | Bayer | 5 tablets | — | — | Discontinued | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 11822-9990-00 | Rite | 10 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 21130-0724-15 | Safeway | 15 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 30142-0724-15 | The | 1 tablet | — | — | FDA listed | — |
| allergy congestion relief 10 mg/1; 240 mg 30142-0846-22 | Kroger | 1 tablet | — | — | FDA listed | — |
| topcare allergy and congestion relief 10 mg/1; 240 mg 36800-0706-22 | Topco | 1 tablet | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 37808-0427-69 | HEB | 10 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 37808-0724-69 | HEB | 10 tablets | — | — | FDA listed | — |
| Allergy Relief-D 240 mg/1; 10 mg 37808-0787-07 | HEB | 5 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 41250-0724-52 | Meijer | 15 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 49035-0488-15 | WAL-MART | 15 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 51660-0491-15 | Ohm | 15 tablets | — | — | Discontinued | — |
| Loratadine and Pseudoephedrine Sulfate 10 mg/1; 240 mg 56062-0724-15 | Publix | 15 tablets | — | — | FDA listed | — |
| Allergy Relief-D 10 mg/1; 240 mg 59779-0726-15 | CVS | 5 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 63187-0305-10 | Proficient | 10 tablets | — | — | FDA listed | — |
| kirkland signature allerclear d 24 hr 10 mg/1; 240 mg 63981-0138-22 | Costco | 1 tablet | — | — | FDA listed | — |
| KIRKLAND SIGNATURE ALLERCLEAR D 24 HR Extended Release 10 mg/1; 240 mg 63981-0724-15 | Kirkland-COSTCO | 15 tablets | — | — | FDA listed | — |
| Loratadine and Pseudoephedrine 10 mg/1; 240 mg 85766-0048-10 | Sportpharm | 10 tablets | — | — | FDA listed | — |
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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
🏛️
2022
On the market since
Dec 2022
📍
2026
Currently FDA-listed
4 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug
This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.
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.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Claritin-D 24 Hour (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 30%
Female · 69%
Unknown · 0%
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 11523-0102-01 You're viewing this | 1 BLISTER PACK in 1 CARTON (11523-0102-1) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2022-12-12 | Active |
| 11523-0102-02 | 1 BLISTER PACK in 1 CARTON (11523-0102-2) / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2022-12-12 | Active |
Pack size FAQ
What quantity is in NDC 11523-0102-01?
NDC 11523-0102-01 is a 10-count package — 1 blister pack in 1 carton / 10 tablet, extended release in 1 blister pack.
What is the difference between NDC 11523-0102-01 and NDC 11523-0102-02?
Both are Claritin-D 24 Hour Loratadine pseudoephedrine sulfate 10 mg; 240 mg Tablet, Extended Release — the drug itself is identical. NDC 11523-0102-01 is the 10-count package, while NDC 11523-0102-02 is the 15 tablets package.
What NDC number is used to bill for this package of Claritin-D 24 Hour Loratadine pseudoephedrine sulfate 10 mg; 240 mg Tablet, Extended Release?
Bill NDC 11523-0102-01 — the 11-digit billing format is 11523010201. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
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
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 FDA registers it as 11523-0102-1, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 11523-0102-01, written without dashes as 11523010201. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 11523-0102-01, the first segment (11523) is the labeler code FDA assigned to Bayer HealthCare LLC.; the middle segment (0102) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Bayer HealthCare LLC.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 15 tablets (11523-0102-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Bayer HealthCare LLC. 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.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
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.
📄 FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing itchy, watery eyes runny nose itching of the nose or throat temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose
⏱️ Dosage and Administration ▾
Directions do not divide, crush, chew or dissolve the tablet adults and children 12 years and over 1 tablet daily with a full glass of water; not more than 1 tablet in 24 hours children under 12 years of age ask a doctor consumers with liver or kidney disease ask a doctor
⚠️ Warnings ▾
Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have heart disease thyroid disease high blood pressure diabetes trouble urinating due to an enlarged prostate gland liver or kidney disease.
Your doctor should determine if you need a different dose. When using this product do not take more than directed. Taking more than directed may cause drowsiness.
Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. symptoms do not improve within 7 days or are accompanied by a fever nervousness, dizziness or sleeplessness occurs If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information store between 20° to 25°C (68° to 77°F) protect from light and store in a dry place
🧪 Active Ingredient ▾
Active ingredient (in each tablet) Purpose Loratadine 10 mg Antihistamine Pseudoephedrine sulfate 240 mg Nasal decongestant
🧪 Inactive Ingredients ▾
Inactive ingredients black iron oxide, candelilla wax powder, Inactive ingredients colloidal silicon dioxide, glyceryl monostearate, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, polysorbate 80, propylene glycol, sodium lauryl sulfate, talc, titanium dioxide
🎯 Purpose ▾
Active ingredient (in each tablet) Purpose Loratadine 10 mg Antihistamine Pseudoephedrine sulfate 240 mg Nasal decongestant
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.