NDC codes

FDA NDC Directory
Product NDC (as listed)62207-889Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62207-0889Add 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
62207-889-4962207088949622070889491000 TABLET, FILM COATED in 1 BOTTLE (62207-889-49)Marketed from Nov 7, 2023
62207-889-5162207088951622070889511 BOTTLE in 1 CARTON (62207-889-51) / 10 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 7, 2023
62207-889-6062207088960622070889608 BLISTER PACK in 1 CARTON (62207-889-60) / 9 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Nov 7, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Fexofenadine Hydrochloride
Generic name (nonproprietary)
fexofenadine hydrochloride
Active ingredients
Fexofenadine hydrochloride — 60 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Granules India LimitedNDC labeler code 62207
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211075
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 62207-889_5447e2c4-49cb-5f8d-e063-6294a90a2457SPL ID 5447e2c4-49cb-5f8d-e063-6294a90a2457SPL set ID e0537b71-fdee-4122-9c09-868ce7352080RxCUI 997420, 997501UNII 2S068B75ZUUPC 0362207891516, 0362207889605, 0362207891585, 0362207889513
Pharmacologic class
Histamine-1 Receptor Antagonist

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

N462207088949 followed by a unit qualifier and the quantity

Package 62207-0889-49. 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)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62207-889

What is NDC 62207-889?
62207-889 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 60 mg/1 tablet, film coated, listed with the FDA by Granules India Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Fexofenadine Hydrochloride.
What is the active ingredient?
Fexofenadine hydrochloride.
Who is the labeler?
Granules India Limited, NDC labeler code 62207. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fexofenadine Hydrochloride?
42 other product NDCs are listed under this name. See all Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Fexofenadine Hydrochloridefexofenadine hydrochloride oralFexofenadine hydrochloride 30 mg/5mLSuspensionOralAurohealth LLC58602-42758602-0427-2058602-0427-24
Fexofenadine HydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralNUVICARE LLC84324-04584324-0045-01
Fexofenadine HydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralYYBA Corp73581-02573581-0025-0173581-0025-0673581-0025-20
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralYYBA Corp73581-02673581-0026-0173581-0026-1073581-0026-20
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralYYBA Corp73581-02773581-0027-0173581-0027-0473581-0027-10+1 more
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1Tablet, Film coatedOralAMZ789 LLC73629-00873629-0008-03
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralNUVICARE LLC84324-00884324-0008-01
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1Tablet, Film coatedOralAMERISOURCE BERGEN46122-77946122-0779-5846122-0779-6146122-0779-66
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralPioneer Life Sciences, LLC72090-01072090-0010-01
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1Tablet, Film coatedOralGranules India Limited62207-89162207-0891-4962207-0891-5162207-0891-58

All 43 Fexofenadine Hydrochloride NDCs

Other NDCs under ANDA 211075

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

FDA NDC Directory listings under ANDA 211075
ProductStrengthForm · routeLabelerProduct NDC
12HR Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralCARDINAL HEALTH70000-0586
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralSafeway, Inc.21130-451
Allergy Relieffexofenadine hclFexofenadine hydrochloride 180 mg/1TabletOralSafeway, Inc.21130-821
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralTOPCO ASSOCIATES LLC36800-653
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralHEB37808-391
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralHEB37808-392
allergy relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralUnited Natural Foods, Inc. dba UNFI41163-292
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralHYVEE INC42507-192
Allergy Relieffexofenadine hclFexofenadine hydrochloride 180 mg/1TabletOralCVS PHARMACY, INC51316-801
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralDISCOUNT DRUG MART53943-392
Allergy Relieffexofenadine hclFexofenadine hydrochloride 180 mg/1TabletOralFamily Dollar (FAMILY WELLNESS)55319-965
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralAAA PHARMACEUTICAL, INC.57344-292
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralAMERIFOODS TRADING COMPANY61504-192
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralCHAIN DRUG MARKETING ASSOCIATION INC63868-334
Allergy Relieffexofenadine hclFexofenadine hydrochloride 180 mg/1TabletOralBest Choice (Valu Merchandisers Company)63941-801
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralMARC GLASSMAN, INC.68998-292
Allergy Relieffexofenadine hclFexofenadine hydrochloride 180 mg/1Capsule, CoatedOralAllegiant Health69168-413
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralCVS PHARMACY69842-492
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralHARRIS TEETER72036-191
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralHARRIS TEETER72036-292

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