NDC codes

FDA NDC Directory
Product NDC (as listed)59556-917Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59556-0917Add 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
59556-917-0159556091701595560917011 BLISTER PACK in 1 CARTON (59556-917-01) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Aug 10, 2021
59556-917-0259556091702595560917022 BLISTER PACK in 1 CARTON (59556-917-02) / 20 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Aug 10, 2021
59556-917-0359556091703595560917033 BLISTER PACK in 1 CARTON (59556-917-03) / 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Aug 10, 2021
59556-917-0459556091704595560917044 BLISTER PACK in 1 CARTON (59556-917-04) / 40 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Aug 10, 2021
59556-917-0559556091705595560917055 BLISTER PACK in 1 CARTON (59556-917-05) / 50 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Aug 10, 2021
59556-917-0659556091706595560917066 BLISTER PACK in 1 CARTON (59556-917-06) / 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Aug 10, 2021

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, Orally disintegrating
Route
Oral
Labeler
Strides Pharma IncNDC labeler code 59556
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213294
Marketing start
Listing expires
Identifiers
Product ID 59556-917_0df1189a-9973-e8b7-e063-6294a90a61a3SPL ID 0df1189a-9973-e8b7-e063-6294a90a61a3SPL set ID 16ab6610-ac99-4714-848d-9377c6bca459RxCUI 311373UNII 7AJO3BO7QN

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

N459556091701 followed by a unit qualifier and the quantity

Package 59556-0917-01. 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 59556-917

What is NDC 59556-917?
59556-917 is the product NDC for Loratadine, Loratadine 10 mg/1 tablet, orally disintegrating, listed with the FDA by Strides Pharma Inc. It has 6 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?
Strides Pharma Inc, NDC labeler code 59556. 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 213294

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

FDA NDC Directory listings under ANDA 213294
ProductStrengthForm · routeLabelerProduct NDC
Alavert AllergyloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralFoundation Consumer Healthcare69536-190
Alavert AllergyloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralFoundation Consumer Healthcare69536-195
AllervarxloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralInnovus Pharmaceuticals, Inc.57483-950
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralDr. Reddy's Laboratories Inc.43598-707
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralDr. Reddy's Laboratories Inc.43598-758
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralCVS PHARMACY, INC51316-503
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralTenshi Kaizen Pvt Ltd72983-501
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralTenshi Kaizen Pvt Ltd72983-503

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