What is NDC 0363-4020?

0363-4020 is the product NDC for Childrens Loratadine ODT (loratadine), Loratadine 10 mg/1 tablet, orally disintegrating, listed with the FDA by WALGREEN CO.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Childrens Loratadine ODT (Loratadine).

WALGREEN CO., NDC labeler code 0363. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Childrens Loratadine ODT?

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.

Childrens Loratadine ODT NDC 0363-4020

NDC codes

FDA NDC Directory

Product NDC (as listed)0363-4020Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00363-4020Add 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
0363-4020-84	0036340208400363402084	3 BLISTER PACK in 1 CARTON (0363-4020-84) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Apr 11, 2018

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Childrens Loratadine ODT
Generic name (nonproprietary): loratadine
Active ingredients: Loratadine — 10 mg/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: WALGREEN CO.NDC labeler code 0363
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208477
Marketing start: Apr 11, 2018
Listing expires: Dec 31, 2027
Identifiers: Product ID 0363-4020_99ea2d7a-6eb5-49a3-bddd-58afafdf8ea7SPL ID 99ea2d7a-6eb5-49a3-bddd-58afafdf8ea7SPL set ID cd597728-35fb-4e43-85ea-84af802e1983RxCUI 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

N400363402084 followed by a unit qualifier and the quantity

Package 00363-4020-84. 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 May 4, 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 0363-4020

What is NDC 0363-4020?: 0363-4020 is the product NDC for Childrens Loratadine ODT (loratadine), Loratadine 10 mg/1 tablet, orally disintegrating, listed with the FDA by WALGREEN CO.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Childrens Loratadine ODT (Loratadine).
What is the active ingredient?: Loratadine.
Who is the labeler?: WALGREEN CO., NDC labeler code 0363. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Childrens Loratadine ODT?: 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 208477

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

FDA NDC Directory listings under ANDA 208477
Product	Strength	Form · route	Labeler	Product NDC
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	WALGREEN CO.	0363-9937
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Rugby Laboratories	0536-1367
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Better Living Brands, LLC	21130-221
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Amerisource Bergen	46122-539
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Wal-Mart Stores, Inc.	49035-806
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	DISCOUNT DRUG MART	53943-035
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Aurohealth LLC	58602-744
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Aurohealth LLC	58602-821
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Aurohealth LLC	58602-830
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Aurohealth LLC	58602-881
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Ahold U.S.A., Inc,	60000-950
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Chain Drug Consortium, LLC	68016-088
Loratadine ODTloratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	CVS Pharmacy, Inc.	69842-085

Childrens Loratadine ODT (Loratadine) NDC 0363-4020