NDC codes

FDA NDC Directory
Product NDC (as listed)69842-052Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69842-0052Add 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
69842-052-1569842005215698420052153 BLISTER PACK in 1 CARTON (69842-052-15) / 5 TABLET in 1 BLISTER PACKMarketed from Apr 1, 2011
69842-052-1869842005218698420052181 CARTON in 1 CARTON (69842-052-18) / 180 TABLET in 1 CARTONMarketed from Feb 1, 2013
69842-052-2969842005229698420052293 BLISTER PACK in 1 CARTON (69842-052-29) / 15 TABLET in 1 BLISTER PACKMarketed from Apr 1, 2011
69842-052-3069842005230698420052301 BOTTLE in 1 CARTON (69842-052-30) / 30 TABLET in 1 BOTTLEMarketed from Apr 1, 2011
69842-052-4569842005245698420052451 BOTTLE in 1 CARTON (69842-052-45) / 45 TABLET in 1 BOTTLEMarketed from Apr 1, 2011
69842-052-7069842005270698420052701 BOTTLE in 1 CARTON (69842-052-70) / 70 TABLET in 1 BOTTLEMarketed from Jan 11, 2019
69842-052-9069842005290698420052901 BOTTLE in 1 CARTON (69842-052-90) / 90 TABLET in 1 BOTTLEMarketed from Apr 1, 2011

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 — 180 mg/1
Dosage form
Tablet
Route
Oral
Labeler
CVS Health Corp.NDC labeler code 69842
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076502
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 69842-052_d9904925-6db2-afaf-c11b-8bbf25249c49SPL ID d9904925-6db2-afaf-c11b-8bbf25249c49SPL set ID 204506d7-7688-fd7e-0aae-142b698848efRxCUI 997420UNII 2S068B75ZU
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

N469842005215 followed by a unit qualifier and the quantity

Package 69842-0052-15. 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 temporarily relieves these symptoms due to hay fever or otherupper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69842-052

What is NDC 69842-052?
69842-052 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by CVS Health Corp.. It has 7 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?
CVS Health Corp., NDC labeler code 69842. 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 60 mg/1Tablet, Film coatedOralGranules India Limited62207-88962207-0889-4962207-0889-5162207-0889-60

All 43 Fexofenadine Hydrochloride NDCs

Other NDCs under ANDA 076502

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

FDA NDC Directory listings under ANDA 076502
ProductStrengthForm · routeLabelerProduct NDC
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralRite Aid Corporation11822-3698
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralSafeway Inc21130-784
Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralFamily Dollar Stores, Inc.55319-917
Fexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralWalgreens Company0363-0783
Fexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralKROGER COMPANY30142-878
Fexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralDr. Reddy's Laboratories Inc.43598-809
Fexofenadine HydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralDr. Reddy's Laboratories Inc.43598-936
Fexofenadine hydrochlorideFexofenadine hydrochloride 30 mg/1TabletOralDr. Reddy's Laboratories Limited55111-782
Fexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralDr. Reddy's Laboratories Limited55111-783
Fexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralDr. Reddy's Laboratories Limited55111-784
Fexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralDollar General55910-111
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralChain Drug Marketing Associate63868-025
Fexofenadine hydrochlorideFexofenadine hydrochloride 60 mg/1TabletOralBluePoint Laboratories68001-439
Fexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralBluePoint Laboratories68001-440
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralChain Drug Consortium, LLC68016-995
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralSam's West Inc.68196-107
Fexofenadine HydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralStrategic Sourcing Services, LLC70677-1009
Non-Drowsy Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralTARGET CORPORATION11673-621
Wal-Fexfexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralWalgreens Company0363-0784

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