What is NDC 68788-8605?

68788-8605 is the product NDC for Loratadine, Loratadine 10 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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?

108 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Loratadine NDC 68788-8605 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-8605Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-8605Add 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
68788-8605-0	68788860500	10 TABLET in 1 BOTTLE (68788-8605-0)Marketed from Mar 13, 2024
68788-8605-1	68788860501	14 TABLET in 1 BOTTLE (68788-8605-1)Marketed from Mar 13, 2024
68788-8605-3	68788860503	30 TABLET in 1 BOTTLE (68788-8605-3)Marketed from Mar 13, 2024
68788-8605-5	68788860505	15 TABLET in 1 BOTTLE (68788-8605-5)Marketed from Mar 13, 2024
68788-8605-9	68788860509	90 TABLET in 1 BOTTLE (68788-8605-9)Marketed from Mar 13, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211718
Marketing start: Mar 13, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 68788-8605_48cbeb9b-de13-4330-97b2-f87fb7e26cb9SPL ID 48cbeb9b-de13-4330-97b2-f87fb7e26cb9SPL set ID d778c4d2-184a-4dc8-9351-66d81d0618f2RxCUI 311372UNII 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

N468788860500 followed by a unit qualifier and the quantity

Package 68788-8605-00. 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 28, 2026.

Indications (excerpt from the label)

USE(S) 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 68788-8605

What is NDC 68788-8605?: 68788-8605 is the product NDC for Loratadine, Loratadine 10 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 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?: Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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?: 108 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Loratadine	Loratadine 10 mg/1	TabletOral	YYBA CORP	73581-229	73581-0229-0173581-0229-03
Loratadine	Loratadine 10 mg/1	TabletOral	AvPAK	50268-777	50268-0777-01
Loratadine	Loratadine 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4103	68788-4103-0068788-4103-0168788-4103-03+2 more
Loratadine	Loratadine 10 mg/1	TabletOral	Safecor Health, LLC	48433-064	48433-0064-20
Loratadine	Loratadine 10 mg/1	TabletOral	Aurobindo Pharma Limited	84386-119	84386-0119-78
Loratadine	Loratadine 10 mg/1	TabletOral	Cabinet Health P.B.C.	82725-0142	82725-0142-0182725-0142-0282725-0142-03+1 more
Loratadine	Loratadine 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0188	55154-0188-00
Loratadine	Loratadine 10 mg/1	TabletOral	Major Pharmaceuticals	0904-7511	00904-7511-61
Loratadine	Loratadine 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8659	68788-8659-0068788-8659-0168788-8659-03+2 more
Loratadine	Loratadine 10 mg/1	Tablet, Orally disintegratingOral	Tenshi Kaizen Pvt Ltd	72983-503	72983-0503-06

All 109 Loratadine NDCs

Other NDCs under ANDA 211718

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

FDA NDC Directory listings under ANDA 211718
Product	Strength	Form · route	Labeler	Product NDC
Loratadine	Loratadine 10 mg/1	TabletOral	Camber Consumer Care Inc	69230-323
Loratadine	Loratadine 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-2551
Loratadine	Loratadine 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-2391
Loratadine 10mg	Loratadine 10 mg/1	TabletOral	Allegiant Health	69168-475
Loratadine	Loratadine 10 mg/1	TabletOral	AvPAK	50268-777