NDC codes

FDA NDC Directory
Product NDC (as listed)58602-702Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58602-0702Add 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
58602-702-04586020702045860207020410 BLISTER PACK in 1 CARTON (58602-702-04) / 10 TABLET in 1 BLISTER PACKMarketed from Feb 10, 2020
58602-702-0558602070205586020702055 BLISTER PACK in 1 CARTON (58602-702-05) / 10 TABLET in 1 BLISTER PACKMarketed from Apr 16, 2018
58602-702-0958602070209586020702091 BOTTLE in 1 CARTON (58602-702-09) / 30 TABLET in 1 BOTTLEMarketed from May 3, 2019
58602-702-1558602070215586020702151 BOTTLE in 1 CARTON (58602-702-15) / 60 TABLET in 1 BOTTLEMarketed from Apr 16, 2018
58602-702-1758602070217586020702171 BOTTLE in 1 CARTON (58602-702-17) / 45 TABLET in 1 BOTTLEMarketed from Apr 16, 2018
58602-702-1958602070219586020702191 BOTTLE in 1 CARTON (58602-702-19) / 90 TABLET in 1 BOTTLEMarketed from Apr 16, 2018
58602-702-2158602070221586020702211 BOTTLE in 1 CARTON (58602-702-21) / 100 TABLET in 1 BOTTLEMarketed from Dec 23, 2019
58602-702-2358602070223586020702231 BOTTLE in 1 CARTON (58602-702-23) / 120 TABLET in 1 BOTTLEMarketed from Oct 4, 2019
58602-702-2958602070229586020702291 BOTTLE in 1 CARTON (58602-702-29) / 150 TABLET in 1 BOTTLEMarketed from Aug 13, 2020
58602-702-3258602070232586020702321 BOTTLE in 1 CARTON (58602-702-32) / 180 TABLET in 1 BOTTLEMarketed from Apr 16, 2018
58602-702-3858602070238586020702381 BOTTLE in 1 CARTON (58602-702-38) / 300 TABLET in 1 BOTTLEMarketed from May 3, 2019
58602-702-3958602070239586020702391 BOTTLE in 1 CARTON (58602-702-39) / 365 TABLET in 1 BOTTLEMarketed from May 3, 2019
58602-702-4058602070240586020702401 BOTTLE in 1 CARTON (58602-702-40) / 500 TABLET in 1 BOTTLEMarketed from Nov 28, 2019
58602-702-4458602070244586020702441 BOTTLE in 1 CARTON (58602-702-44) / 400 TABLET in 1 BOTTLEMarketed from Jul 26, 2019
58602-702-5458602070254586020702541 BOTTLE in 1 CARTON (58602-702-54) / 70 TABLET in 1 BOTTLEMarketed from Oct 4, 2019
58602-702-6058602070260586020702601 BLISTER PACK in 1 CARTON (58602-702-60) / 5 TABLET in 1 BLISTER PACKMarketed from Apr 16, 2018
58602-702-6758602070267586020702672 BLISTER PACK in 1 CARTON (58602-702-67) / 10 TABLET in 1 BLISTER PACKMarketed from Apr 16, 2018
58602-702-8158602070281586020702811 BOTTLE in 1 CARTON (58602-702-81) / 108 TABLET in 1 BOTTLEMarketed from Apr 16, 2018
58602-702-8358602070283586020702831 BLISTER PACK in 1 CARTON (58602-702-83) / 10 TABLET in 1 BLISTER PACKMarketed from Apr 16, 2018
58602-702-8458602070284586020702843 BLISTER PACK in 1 CARTON (58602-702-84) / 10 TABLET in 1 BLISTER PACKMarketed from Apr 16, 2018

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)
Loratadine
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Aurohealth LLCNDC labeler code 58602
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208314
Marketing start
Listing expires
Identifiers
Product ID 58602-702_94169799-0508-439b-93c5-132b9e6ae767SPL ID 94169799-0508-439b-93c5-132b9e6ae767SPL set ID 196da80c-3dbb-40c7-ac93-8a57d6acb1c3RxCUI 311372UNII 7AJO3BO7QNUPC 0358602702175

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

N458602070204 followed by a unit qualifier and the quantity

Package 58602-0702-04. 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 other upper 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 58602-702

What is NDC 58602-702?
58602-702 is the product NDC for Loratadine, Loratadine 10 mg/1 tablet, listed with the FDA by Aurohealth LLC. It has 20 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Loratadine.
What is the active ingredient?
Loratadine.
Who is the labeler?
Aurohealth LLC, NDC labeler code 58602. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Loratadine?
109 other product NDCs are listed under this name. See all Loratadine 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 Loratadine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LoratadineLoratadine 10 mg/1TabletOralYYBA CORP73581-22973581-0229-0173581-0229-03
LoratadineLoratadine 10 mg/1TabletOralAvPAK50268-77750268-0777-01
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-410368788-4103-0068788-4103-0168788-4103-03+2 more
LoratadineLoratadine 10 mg/1TabletOralSafecor Health, LLC48433-06448433-0064-20
LoratadineLoratadine 10 mg/1TabletOralAurobindo Pharma Limited84386-11984386-0119-78
LoratadineLoratadine 10 mg/1TabletOralCabinet Health P.B.C.82725-014282725-0142-0182725-0142-0282725-0142-03+1 more
LoratadineLoratadine 10 mg/1TabletOralCardinal Health 107, LLC55154-018855154-0188-00
LoratadineLoratadine 10 mg/1TabletOralMajor Pharmaceuticals0904-751100904-7511-61
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-865968788-8659-0068788-8659-0168788-8659-03+2 more
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralTenshi Kaizen Pvt Ltd72983-50372983-0503-06

All 110 Loratadine NDCs

Other NDCs under ANDA 208314

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

FDA NDC Directory listings under ANDA 208314
ProductStrengthForm · routeLabelerProduct NDC
365 Whole Foods Market LoratadineloratadineLoratadine 10 mg/1TabletOralWhole Foods Market, Inc.42681-0053
ALLERGY RELIEF 10mgloratadineLoratadine 10 mg/1TabletOralYYBA CORP73581-203
Amazon Basic Care Allergy ReliefloratadineLoratadine 10 mg/1TabletOralAmazon.com Services LLC72288-452
CONTAC AllergyloratadineLoratadine 10 mg/1TabletOralVespyr Brands LLC71179-010
LoratadineLoratadine 10 mg/1TabletOralWALGREEN CO.0363-9603
LoratadineLoratadine 10 mg/1TabletOralMajor Pharmaceuticals0904-7426
LoratadineLoratadine 10 mg/1TabletOralKROGER COMPANY30142-066
LoratadineLoratadine 10 mg/1TabletOralA-S Medication Solutions50090-7752
LoratadineLoratadine 10 mg/1TabletOralA-S Medication Solutions50090-7753
LoratadineLoratadine 10 mg/1TabletOralMcLane Company, Inc.57243-200
LoratadineLoratadine 10 mg/1TabletOralAurohealth LLC58602-831
LoratadineLoratadine 10 mg/1TabletOralAurohealth LLC58602-847
LoratadineLoratadine 10 mg/1TabletOralWinco Foods, LLC.67091-408
LoratadineLoratadine 10 mg/1TabletOralBluePoint Laboratories68001-438
LoratadineLoratadine 10 mg/1TabletOralChain Drug Consortium, LLC68016-094
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4103
LoratadineLoratadine 10 mg/1TabletOralCVS Pharmacy, Inc.69842-242
LoratadineLoratadine 10 mg/1TabletOralCardinal Health70000-0583
LoratadineLoratadine 10 mg/1TabletOralYYBA CORP73581-229
LoratadineLoratadine 10 mg/1TabletOralAurobindo Pharma Limited84386-119

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