What is NDC 73581-230?

73581-230 is the product NDC for LORATADINE ALLERGY RELIEF 10mg (loratadine), Loratadine 10 mg/1 tablet, listed with the FDA by YYBA CORP. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

LORATADINE ALLERGY RELIEF 10mg (Loratadine).

YYBA CORP, NDC labeler code 73581. 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 ALLERGY RELIEF 10mg?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

LORATADINE ALLERGY RELIEF 10mg NDC 73581-230

NDC codes

FDA NDC Directory

Product NDC (as listed)73581-230Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73581-0230Add 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 NDC	11-digit (billing)	Package	Copy
73581-230-01	7358102300173581023001	100 TABLET in 1 BOTTLE (73581-230-01)Marketed from Apr 15, 2022
73581-230-36	7358102303673581023036	365 TABLET in 1 BOTTLE (73581-230-36)Marketed from Apr 15, 2022

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 ALLERGY RELIEF 10mgSuffix: 10mg
Generic name (nonproprietary): loratadine
Active ingredients: Loratadine — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: YYBA CORPNDC labeler code 73581
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210722
Marketing start: Apr 15, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 73581-230_0e135981-fabe-f255-e063-6394a90ae356SPL ID 0e135981-fabe-f255-e063-6394a90ae356SPL set ID dcb63e1b-d499-2e84-e053-2995a90af5c7RxCUI 311372UNII 7AJO3BO7QNUPC 0373581203017

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

N473581023001 followed by a unit qualifier and the quantity

Package 73581-0230-01. 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 Jan 3, 2024.

Indications (excerpt from the label)

Uses Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes 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 73581-230

What is NDC 73581-230?: 73581-230 is the product NDC for LORATADINE ALLERGY RELIEF 10mg (loratadine), Loratadine 10 mg/1 tablet, listed with the FDA by YYBA CORP. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: LORATADINE ALLERGY RELIEF 10mg (Loratadine).
What is the active ingredient?: Loratadine.
Who is the labeler?: YYBA CORP, NDC labeler code 73581. 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 ALLERGY RELIEF 10mg?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 210722

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

FDA NDC Directory listings under ANDA 210722
Product	Strength	Form · route	Labeler	Product NDC
Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	Grocery Outlet, Inc	85828-193
Loratadine	Loratadine 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-2529
Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	AAA PHARMACEUTICAL, INC.	57344-193
Green Guard 24 Hour Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	Unifirst First Aid Corporation	47682-117
XL - 3 Allergy	Loratadine 10 mg/1	TabletOral	Selder, S.A. de C.V.	63654-415
Loratadine	Loratadine 10 mg/1	TabletOral	Bi-Mart	37835-621
Loratadine	Loratadine 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3596
McKesson Loradatineloratainde	Loratadine 10 mg/1	TabletOral	McKesson Medical Surgical	68599-4785
Loratadine	Loratadine 10 mg/1	TabletOral	Safeway, Inc	21130-780
Loratadine	Loratadine 10 mg/1	TabletOral	Advanced Rx LLC	80513-711
Loratadine	Loratadine 10 mg/1	TabletOral	Granules Pharmaceuticals Inc.	70010-162
ValuMeds Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	Cabinet Health P.B.C.	82725-1042
Loratadine	Loratadine 10 mg/1	TabletOral	Spirit Pharmaceuticals LLC	68210-4110
Loratadine	Loratadine 10 mg/1	TabletOral	Granules India Limited	62207-787
Medique Loradamedloratadine	Loratadine 10 mg/1	TabletOral	Unifirst First Aid Corporation	47682-403
Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	Dr. Reddy's Laboratories Inc.	75907-434
Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	Allegiant Health	69168-414
Allergy Reliefloratadine	Loratadine 10 mg/1	TabletOral	Valu Merchandisers Company	63941-193
Loratadine	Loratadine 10 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-831
Non-Drowsy Allergy Relief, 24-7 Lifeloratadine tablet	Loratadine 10 mg/1	TabletOral	Lil' Drug Store Products, Inc.	66715-6551

Showing 20 of 39.

LORATADINE ALLERGY RELIEF 10mg (Loratadine) NDC 73581-230