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Fexofenadine Hydrochloride 60 mg Tablet, Film Coated, 1,000-count — NDC 62207-0889-49 package photo

Fexofenadine Hydrochloride 60 mg Tablet, Film Coated, 1,000-count

by Granules India Limited · 1000 TABLET, FILM COATED in 1 BOTTLE (62207-889-49)
NDC 62207-0889-49
🏷️ FDA NDC (as labeled) 62207-889-49 billing pads the product segment with a zero
This package
Contains1,000-count Pack sizes3 compare ↓
Also comes in: 9 tablets 62207-0889-60 10 tablets 62207-0889-51
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 →

This page is curated, coded, and maintained by

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

🆔 Identity & classification

FDA NDC (as labeled) 62207-889-49
Product NDC 62207-889
11-digit billing NDC 62207088949
RxCUI 997420, 997501
UNII 2S068B75ZU
UPC 0362207891516, 0362207889605, 0362207891585, 0362207889513
Application # ANDA211075
SPL Set ID e0537b71-fdee-4122-9c09-868ce7352080
Established class (EPC) Histamine-1 Receptor Antagonist
Mechanism of action Histamine H1 Receptor Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-11-07
Route ORAL
Dosage form TABLET, FILM COATED
Substance FEXOFENADINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 62207-889-49 — 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 → 62207-0889-49. 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 Histamine-1 Receptor Antagonist class.

Pharmacologic class Histamine-1 Receptor Antagonist
Drug family (ATC) Other antihistamines for systemic use
How it works Histamine H1 Receptor Antagonists
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

LabelerGranules India Limited
Application holderGRANULES INDIA LTD
FDA applicationANDA211075 (ANDA)
Labeler code62207
First marketedNov 2023
Product typeHuman Otc Drug
Portfolio93 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

📗 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.

💊 What it looks like

Color orange
ShapeCapsule
ImprintG6
Size17 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 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.
Try another pack size: 9 tablets 10 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
fexofenadine hcl 60 mg 00904-7192-40 Major 500 tablets $0.153 — Availability likely —
Fexofenadine hydrochloride 60 mg 55111-0783-01 Dr. 100 tablets $0.153 — Availability likely —
Fexofenadine hydrochloride 60 mg 68001-0439-00 BluePoint 100 tablets $0.153 — Availability likely —
Fexofenadine HCl 60 mg 69230-0201-05 Camber 500 tablets $0.153 — Availability likely —
12HR Allergy Relief 60 mg 70000-0586-01 CARDINAL 12 tablets $0.153 — Availability likely —
Allergy Relief 60 mg 70677-1008-01 Strategic 24 tablets $0.153 — Discontinued —
Allergy Relief 60 mg 83324-0009-12 Chain 12 tablets $0.153 — Availability likely —
Fexofenadine hydrochloride 60 mg 00363-0783-24 Walgreens 24 tablets — — FDA listed —
Fexofenadine HCL 60 mg 00363-9765-24 Walgreens 24 tablets — — FDA listed —
Fexofenadine HCl 60 mg 11822-7652-04 Rite 24 tablets — — FDA listed —
Allergy Relief 60 mg 11822-9995-01 Rite 24 tablets — — Discontinued —
Fexofenadine Hydrochloride 60 mg 30142-0091-12 Kroger 12 tablets — — Discontinued —
Allergy Relief 60 mg 37808-0391-02 HEB 12 tablets — — FDA listed —
Allegra Allergy 60 mg 41167-4131-02 Chattem, 12 tablets — — FDA listed —
Fexofenadine Hydrochloride 60 mg 43598-0936-01 Dr. 100 tablets — — FDA listed —
fexofenadine hcl 60 mg 50228-0201-01 ScieGen 30 tablets — — FDA listed —
Crcle Fexofenadine Hydrochloride 60 mg 57483-0230-01 Innovus 100 tablets — — FDA listed —
Fexofenadine Hydrochloride 60 mg 62207-0765-49 Granules 1000 tablets — — FDA listed —
Fexofenadine Hydrochloride 60 mgthis 62207-0889-49 Granules 1000 tablets — — FDA listed —
Allergy Relief 60 mg 63548-0663-05 PLD 500 tablets — — FDA listed —
Allergy Relief 60 mg 63868-0819-12 Chain 12 tablets — — Discontinued —
Allergy Relief Non Drowsy 60 mg 69168-0437-06 Allegiant 120 tablets — — FDA listed —
Fexofenadine HCL 60 mg 69230-0301-01 Camber 100 tablets — — FDA listed —
Allergy Relief 60 mg 69842-0492-02 CVS 12 tablets — — FDA listed —
fexofenadine hcl 60 mg 71335-2165-01 Bryant 30 tablets — — FDA listed —
fexofenadine hcl 60 mg 71399-8659-01 AKRON 100 tablets — — FDA listed —
Allergy Relief 60 mg 72036-0191-03 HARRIS 288 tablets — — FDA listed —
Gencare-Allergy Relief 60 mg 72090-0068-01 Pioneer 100 tablets — — FDA listed —
Fexofenadine HCL 60 mg 73581-0010-01 YYBA 10 tablets — — FDA listed —
Fexofenadine Hydrochloride 60 mg 73581-0025-01 YYBA 10 tablets — — FDA listed —
Allergy Relief 60 mg 73581-0103-10 YYBA 100 tablets — — FDA listed —
fexofenadine hcl 60 mg 77771-0201-01 Radha 100 tablets — — FDA listed —
Fexofenadine Hydrochloride 60 mg 84324-0045-01 NUVICARE 60 tablets — — FDA listed —
Fexofenadine Hydrochloride 60 mg 58602-0877-09 Aurohealth 30 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

🏛️
2023
On the market since
Nov 2023
📍
2026
Currently FDA-listed
3 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
62207-0889-49 You're viewing this 1000 TABLET, FILM COATED in 1 BOTTLE (62207-889-49) 2023-11-07 Active
62207-0889-51 1 BOTTLE in 1 CARTON (62207-889-51) / 10 TABLET, FILM COATED in 1 BOTTLE 2023-11-07 Active
62207-0889-60 8 BLISTER PACK in 1 CARTON (62207-889-60) / 9 TABLET, FILM COATED in 1 BLISTER PACK 2023-11-07 Active

Pack size FAQ

What quantity is in NDC 62207-0889-49?
NDC 62207-0889-49 is a 1,000-count package — 1000 tablet, film coated in 1 bottle.
What is the difference between NDC 62207-0889-49 and NDC 62207-0889-51?
Both are Fexofenadine Hydrochloride 60 mg Tablet, Film Coated — the drug itself is identical. NDC 62207-0889-49 is the 1,000-count package, while NDC 62207-0889-51 is the 10 tablets package.
What NDC number is used to bill for this package of Fexofenadine Hydrochloride 60 mg Tablet, Film Coated?
Bill NDC 62207-0889-49 — the 11-digit billing format is 62207088949. 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 ✓ Available
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 62207-889-49, 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: 62207-0889-49, written without dashes as 62207088949. 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 62207-0889-49, the first segment (62207) is the labeler code FDA assigned to Granules India Limited; the middle segment (0889) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (49) 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 Granules India Limited. 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 2 other package presentations of this same product, including 9 tablets (62207-0889-60), 10 tablets (62207-0889-51). 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?
Granules India 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.
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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 23 words ▾

Uses reduces hives and relieves itching due to hives (urticaria). This product will not prevent hives or an allergic skin reaction from occurring.

⏱️ Dosage and Administration 82 words ▾

Directions adults and children 12 years of age and over take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hours (for 60 mg) take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours (for 180 mg) children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor

⚠️ Warnings ~2 min read ▾

Warnings Severe Allergy Warning: Get emergency help immediately if you have hives along with any of the following symptoms: trouble swallowing dizziness or loss of consciousness swelling of tongue swelling in or around mouth trouble speaking wheezing or problems breathing drooling These symptoms may be signs of anaphylactic shock. This condition can be life threatening if not treated by a health professional immediately . Symptoms of anaphylactic shock may occur when hives first appear or up to a few hours later.

Not a Substitute for Epinephrine. If your doctor has prescribed an epinephrine injector for “anaphylaxis” or severe allergy symptoms that could occur with your hives, never use this product as a substitute for the epinephrine injector. If you have been prescribed an epinephrine injector, you should carry it with you at all times.

Do not use to prevent hives from any known cause such as: foods insect stings medicines latex or rubber gloves because this product will not stop hives from occurring. Avoiding the cause of your hives is the only way to prevent them. Hives can sometimes be serious.

If you do not know the cause of your hives, see your doctor for a medical exam. Your doctor may be able to help you find a cause. if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose. hives that are an unusual color, look bruised or blistered hives that do not itch When using this product do not take more than directed do not take at the same time as aluminum or magnesium antacids do not take with fruit juices (see Directions) Stop use and ask a doctor if an allergic reaction to this product occurs.

Seek medical help right away. symptoms do not improve after 3 days of treatment the hives have lasted more than 6 weeks 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.

🧪 Active Ingredient 21 words ▾

Active ingredient (in each tablet) Fexofenadine HCl USP, 60 mg (for 60 mg) Fexofenadine HCl USP, 180 mg (for 180 mg)

🧪 Inactive Ingredients 28 words ▾

Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, macrogol, magnesium stearate, microcrystalline cellulose, pregelatinized starch, titanium dioxide.

🎯 Purpose 2 words ▾

Purpose Antihistamine

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 62207-0840-71 · Granules 62207-0891-49 · Granules →
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.