What is NDC 72090-051?

72090-051 is the product NDC for Gencare-Allergy Relief Loratadine Tablets, 10 mg, Loratadine 10 mg/1 tablet, listed with the FDA by Pioneer Life Sciences, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Gencare-Allergy Relief Loratadine Tablets, 10 mg (Loratadine).

Pioneer Life Sciences, LLC, NDC labeler code 72090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gencare-Allergy Relief Loratadine Tablets, 10 mg?

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.

NDC 72090-051

NDC codes

FDA NDC Directory

Product NDC (as listed)72090-051Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72090-0051Add 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
72090-051-01	7209000510172090005101	300 TABLET in 1 BOTTLE (72090-051-01)Marketed from Jun 30, 2025

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): Gencare-Allergy Relief Loratadine Tablets, 10 mg
Generic name (nonproprietary): loratadine
Active ingredients: Loratadine — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Pioneer Life Sciences, LLCNDC labeler code 72090
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214684
Marketing start: Jun 30, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 72090-051_e45f0822-5a81-429b-9518-a9c423d6f9c3SPL ID e45f0822-5a81-429b-9518-a9c423d6f9c3SPL set ID 647dc957-4aee-48f6-bb77-e82d3b380e80RxCUI 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

N472090005101 followed by a unit qualifier and the quantity

Package 72090-0051-01. 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 Jun 30, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves these symptoms due to hay fever or other 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 72090-051

What is NDC 72090-051?: 72090-051 is the product NDC for Gencare-Allergy Relief Loratadine Tablets, 10 mg, Loratadine 10 mg/1 tablet, listed with the FDA by Pioneer Life Sciences, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gencare-Allergy Relief Loratadine Tablets, 10 mg (Loratadine).
What is the active ingredient?: Loratadine.
Who is the labeler?: Pioneer Life Sciences, LLC, NDC labeler code 72090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gencare-Allergy Relief Loratadine Tablets, 10 mg?: 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 214684

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

FDA NDC Directory listings under ANDA 214684
Product	Strength	Form · route	Labeler	Product NDC
CVS Loratadineloratadine	Loratadine 10 mg/1	TabletOral	CVS Pharmacy	51316-184
Loratadine	Loratadine 10 mg/1	TabletOral	Rising Pharmaceuticals, Inc	16571-822
Loratadine	Loratadine 10 mg/1	TabletOral	A-S Medication Solutions	50090-8075
Loratadine	Loratadine 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-5308
Loratadine	Loratadine 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc	68788-8616
Loratadine	Loratadine 10 mg/1	TabletOral	Strategic Sourcing Services, LLC	70677-1240
Loratadine	Loratadine 10 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0352
Loratadine	Loratadine 10 mg/1	TabletOral	Gobrands, Inc	82501-1580
Loratadine	Loratadine 10 mg/1	TabletOral	Cabinet Health P.B.C.	82725-0142
Nuvicare-Allergy Relief Loratadine Tablets, 10 mgloratadine	Loratadine 10 mg/1	TabletOral	NUVICARE LLC	84324-027
ValuMeds Allergy Relief Loratadineloratadine	Loratadine 10 mg/1	TabletOral	Cabinet Health P.B.C.	82725-1142

Gencare-Allergy Relief Loratadine Tablets, 10 mg (Loratadine) NDC 72090-051