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Fexofenadine hydrochloride 180 mg Tablet, 1,500-count — NDC 43598-577-89 (Billing 43598-0577-89)

by Dr. Reddy's Laboratories Inc. · 1500 TABLET in 1 POUCH

This is a package of 1,500 tablets of Fexofenadine hydrochloride 180 mg Tablet from Dr. Reddy's Laboratories Inc., marketed since Jul 2016 and currently FDA-listed. It is this product's only package size.

NDC 43598-0577-89
🏷️ FDA NDC (as labeled) 43598-577-89 billing pads the product segment with a zero
On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 43598-577-89
Product NDC 43598-577
11-digit billing NDC 43598057789
SPL Set ID aa0f3f57-5f07-9e13-ad79-094c7ec9c6d3
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-07-25
Dosage form TABLET
Substance FEXOFENADINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 43598-577-89 — a 5-3-2 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 product segment → 43598-0577-89. 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
  • Fexofenadine is an antihistamine that relieves common allergy symptoms — things like a runny nose, sneezing, itchy or watery eyes, and an itchy nose or throat caused by hay fever o...
  • The FDA labels for fexofenadine do not list drowsiness as a side effect in the consumer sections provided. That said, everyone responds a little differently, so pay attention to ho...
  • You'll want to be careful here. The label says not to take fexofenadine at the same time as aluminum or magnesium antacids — the kind used for heartburn or upset stomach — and to a...
  • Can I take fexofenadine with my antacids or a glass of orange juice?
📖 Read our full Fexofenadine guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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 eachPer 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
43598-0577-89 You're viewing this Main listing 1500 TABLET in 1 POUCH — — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Fexofenadine hydrochloride 180 mg 68001-0440-00 BluePoint 100 tablets $0.230 — Availability likely —
Fexofenadine Hydrochloride 180 mg 70677-1009-01 Strategic 15 tablets $0.230 — Availability likely —
Allergy Relief 180 mg 83324-0095-15 CHAIN 15 tablets $0.230 — Availability likely —
Leader 24HR Allergy Relief 180 mg 70000-0725-01 Cardinal 30 tablets $0.230 — Availability likely —
24HR Allergy Relief 180 mg 70000-0726-01 CARDINAL 180 tablets $0.230 — Availability likely —
Fexofenadine hydrochloride 180 mg 55111-0784-01 Dr. 100 tablets $0.230 — Availability likely —
Allergy Relief 180 mg 46122-0462-22 AMERISOURCEBERGEN 15 tablets $0.230 — Discontinued —
Fexofenadine Hydrochloride 180 mg 46122-0779-58 AMERISOURCE 5 tablets $0.230 — Availability likely —
Fexofenadine Hydrochloride 180 mg 51660-0998-30 OHM 30 tablets $0.230 — Availability likely —
24HR Allergy Relief 180 mg 70000-0361-01 LEADER/ 15 tablets $0.241 — Discontinued —
Fexofenadine Hydrochloride 180 mg 45802-0847-78 Padagis 100 tablets $0.257 — FDA listed —
Fexofenadine hydrochloride 180 mg 00904-6711-10 MAJOR 15 tablets $0.265 — Discontinued —
Fexofenadine hydrochloride 180 mg 10202-0229-66 7-eleven 10 tablets — — FDA listed —
Allergy Relief 180 mg 37808-0392-03 HEB 15 tablets — — FDA listed —
allergy relief 180 mg 37808-0847-22 H 1 tablet — — Discontinued —
Allergy Relief 180 mg 53943-0392-04 DISCOUNT 30 tablets — — FDA listed —
dg health aller ease 180 mg 55910-0609-46 Dolgencorp 1 tablet — — FDA listed —
allergy relief 180 mg 56062-0847-22 Publix 1 tablet — — FDA listed —
Allergy Relief 180 mg 68998-0292-04 MARC 30 tablets — — FDA listed —
Allergy Relief 180 mg 72476-0192-04 RETAIL 30 tablets — — FDA listed —
Wal-Fex 180 mg 00363-0784-07 Walgreens 5 tablets — — FDA listed —
Allergy Relief 180 mg 11822-3698-00 Rite 15 tablets — — FDA listed —
Allergy Relief 180 mg 21130-0784-29 Safeway 15 tablets — — FDA listed —
Allergy Relief 180 mg 36800-0653-03 TOPCO 15 tablets — — FDA listed —
allergy relief 180 mg 41163-0292-03 United 15 tablets — — FDA listed —
Allergy Relief 180 mg 54257-0170-02 Magno-Humphries, 100 tablets — — FDA listed —
Allergy Relief 180 mg 55319-0917-15 Family 15 tablets — — FDA listed —
Crcle Fexofenadine Hydrochloride 180 mg 57483-0240-02 Innovus 150 tablets — — FDA listed —
Allergy Relief 180 mg 61504-0192-03 AMERIFOODS 15 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 63868-0025-30 Chain 30 tablets — — FDA listed —
kirkland signature aller fex 180 mg 63981-0847-48 Costco 180 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 68016-0995-03 Chain 30 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 68196-0107-15 Sam's 150 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 71205-0739-30 Proficient 30 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 71309-0091-01 Safrel 100 tablets — — FDA listed —
Nuvicare Hives Relief 180 mg 84324-0031-01 NUVICARE 30 tablets — — FDA listed —
Allergy Relief 180 mg 84324-0040-01 NUVICARE 4 tablets — — FDA listed —
Allegra Allergy 180 mg 41167-4120-00 Chattem, 5 tablets — — FDA listed —
Allegra Allergy 180 mg 41167-4124-00 Chattem, 90 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 73629-0008-03 AMZ789 30 tablets — — FDA listed —
allergy relief 180 mg 79481-0847-00 Meijer, 1 tablet — — FDA listed —
ValuMeds Non-Drowsy Allergy Relief Fexofenadine HCl 180 mg 82725-1202-01 Cabinet 100 tablets — — FDA listed —
Cabinet Allergy Relief Fexofenadine 180 mg 82725-3002-03 Cabinet 30 tablets — — FDA listed —
berkley jensen allergy relief 180 mg 68391-0847-47 BJWC 150 tablets — — FDA listed —
ValuMeds 24-Hour Allergy Relief 180 mg 82725-1002-01 Cabinet 100 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 62207-0623-97 Granules 40000 tablets — — FDA listed —
Non-Drowsy Allergy Relief 180 mg 11673-0621-01 TARGET 150 tablets — — FDA listed —
Allergy Relief 180 mg 21130-0451-15 Safeway, 15 tablets — — FDA listed —
Allegra Allergy 180 mg 41167-4122-00 Chattem, 8 tablets — — FDA listed —
CVS Fexofenadine Hydrochloride 180 mg 51316-0183-00 CVS 180 tablets — — FDA listed —
Allergy Relief 180 mg 57344-0292-02 AAA 5 tablets — — FDA listed —
Allergy Relief 180 mg 72036-0292-03 HARRIS 15 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 73581-0027-01 YYBA 10 tablets — — FDA listed —
Allergy Relief 180 mg 81522-0192-09 FSA 90 tablets — — FDA listed —
Goodmeds Non Drowsy Allergy Relief 180 mg 82725-4202-01 Cabinet 120 tablets — — FDA listed —
Fexofenadine hydrochloride 180 mgthis 43598-0577-89 Dr. 1500 tablets — — FDA listed —
Allergy Relief 180 mg 42507-0192-07 HYVEE 60 tablets — — FDA listed —
Allegra Allergy, Travel BASIX 180 mg 66715-6507-02 Lil' 1 tablet — — FDA listed —
Fexofenadine Hydrochloride 180 mg 72090-0010-01 Pioneer 90 tablets — — FDA listed —
Basic Care Allergy 180 mg 72288-0537-72 Amazon.com 60 tablets — — FDA listed —
Allergy Relief 180 mg 73581-0011-80 YYBA 100 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 82725-0102-02 Cabinet 40000 tablets — — FDA listed —
Fexofenadine hydrochloride 180 mg 30142-0878-15 KROGER 15 tablets — — FDA listed —
topcare allergy relief 180 mg 36800-0691-13 Topco 1 tablet — — Discontinued —
allergy relief 180 mg 42507-0847-39 HyVee 30 tablets — — FDA listed —
exchange select aller ease 180 mg 55301-0847-39 Army 30 tablets — — FDA listed —
Allegra Allergy 180 mg 67751-0033-02 Navajo 1 tablet — — FDA listed —
Basic Care Allergy 180 mg 72288-0722-01 Amazon.com 70 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 84324-0008-01 NUVICARE 18 tablets — — FDA listed —
Allegra Allergy 180 mg 41167-4121-01 Chattem, 60 tablets — — FDA listed —
Allegra Hives 24hr 180 mg 41167-4126-04 Chattem, 30 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 51316-0800-08 CVS 180 tablets — — FDA listed —
Allergy Relief 180 mg 63868-0334-15 CHAIN 15 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 68210-2210-01 SPIRIT 100 tablets — — FDA listed —
allergy relief 180 mg 00363-7011-39 Walgreen 30 tablets — — FDA listed —
good sense aller ease 180 mg 00113-0847-22 L. 1 tablet — — FDA listed —
Fexofenadine hydrochloride 180 mg 55910-0111-30 Dollar 30 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 62207-0766-35 Granules 25000 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 69842-0052-02 CVS 2 tablets — — Discontinued —
Allergy Relief 180 mg 85828-0192-03 Grocery 15 tablets — — FDA listed —
equate allergy relief 180 mg 49035-0366-02 Walmart 120 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 68210-4090-01 SPIRIT 100 tablets — — FDA listed —
Gencare Hives Relief 180 mg 72090-0058-01 Pioneer 48 tablets — — FDA listed —
careone allergy relief 180 mg 72476-0847-22 Retail 1 tablet — — FDA listed —
Fexofenadine Hydrochloride 180 mg 73581-0026-01 YYBA 10 tablets — — FDA listed —
Allegra Allergy 180 mg 50090-1234-00 A-S 30 tablets — — FDA listed —
Allergy Relief 180 mg 69842-0914-01 CVS 70 tablets — — FDA listed —
basic care allergy 180 mg 72288-0847-39 Amazon.com 30 tablets — — FDA listed —
up and up non drowsy allergy relief 180 mg 82442-0300-72 Target 60 tablets — — FDA listed —
Allegra Allergy 24 hour 180 mg 85237-1920-01 Select 1 tablet — — FDA listed —
fexofenadine hydrochloride 180 mg 10888-8251-01 Patheon 54000 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 72091-0010-00 PLS 40000 tablets — — FDA listed —
Fexofenadine hydrochloride 180 mg 43598-0809-18 Dr. 180 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 62207-0891-49 Granules 1000 tablets — — FDA listed —
Allegra Allergy 180 mg 66715-9707-01 Lil' 1 tablet — — FDA listed —
Allergy Relief 180 mg 68016-0887-15 CHAIN 15 tablets — — Discontinued —
Allergy Relief 180 mg 00363-1847-39 Walgreen 30 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 00615-8648-39 NCS 30 tablets — — FDA listed —
Allergy Relief 180 mg 30142-0856-62 Kroger 24 tablets — — FDA listed —
Hives Relief 180 mg 00363-4071-39 Walgreen 30 tablets — — FDA listed —
Fexofenadine Hydrochloride 180 mg 58602-0878-09 Aurohealth 30 tablets — — FDA listed —
Allergy 180 mg 72288-0716-00 Amazon.com 150 tablets — — FDA listed —
Allergy Relief 180 mg 37835-0602-09 Bi-Mart 90 tablets — — 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

🏛️
2016
On the market since
Jul 2016
📍
2026
Currently FDA-listed
10 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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.

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

LabelerDr. Reddy's Laboratories Inc.
Labeler code43598
First marketedJul 2016
Product typeDrug For Further Processing
Portfolio160 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.

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 ↗

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 Fexofenadine hydrochloride — the ingredient across all brands.

Top reported reactions

Headache969
Fatigue954
Pruritus911
Nausea857
Diarrhoea766
Extra Dose Administered722
Dizziness720

Age at onset

Neonate6
Infant8
Child193
Adolescent247
Adult7,080
Elderly2,710

Reporter sex

21,660 reports
Male · 31%
Female · 69%
Unknown · 0%

Serious outcomes

Hospitalization2,929
Death693
Life-threatening353
Disabling346
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,118 1,274
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.

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: Dr. Reddy's Laboratories Inc. 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 Dr. Reddy's Laboratories Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Dr. Reddy's Laboratories Inc. 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.
← 43598-0576-30 · Dr.Reddys 43598-0578-30 · Dr.Reddys →
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.