What is NDC 66715-6458?

66715-6458 is the product NDC for Zantac 360, Travel BASIX, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Lil' Drug Store Products, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Zantac 360, Travel BASIX (Famotidine tablet, film-coated).

Lil' Drug Store Products, Inc, NDC labeler code 66715. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Zantac 360, Travel BASIX?

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.

Zantac 360, Travel BASIX NDC 66715-6458

NDC codes

FDA NDC Directory

Product NDC (as listed)66715-6458Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66715-6458Add 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
66715-6458-2	6671564580266715645802	1 BLISTER PACK in 1 CARTON (66715-6458-2) / 2 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Oct 11, 2022

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): Zantac 360, Travel BASIX
Generic name (nonproprietary): famotidine tablet, film-coated
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Lil' Drug Store Products, IncNDC labeler code 66715
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206531
Marketing start: Oct 11, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 66715-6458_274bc24b-823e-516d-e063-6394a90a2680SPL ID 274bc24b-823e-516d-e063-6394a90a2680SPL set ID ea38535a-c9db-d03f-e053-2a95a90adf2dRxCUI 310273, 2609246UNII 5QZO15J2Z8
Pharmacologic class: Histamine-2 Receptor Antagonist

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

N466715645802 followed by a unit qualifier and the quantity

Package 66715-6458-02. 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 Nov 19, 2024.

Indications (excerpt from the label)

Uses Uses relieves heartburn associated with acid indigestion and sour stomach prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66715-6458

What is NDC 66715-6458?: 66715-6458 is the product NDC for Zantac 360, Travel BASIX, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Lil' Drug Store Products, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Zantac 360, Travel BASIX (Famotidine tablet, film-coated).
What is the active ingredient?: Famotidine.
Who is the labeler?: Lil' Drug Store Products, Inc, NDC labeler code 66715. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Zantac 360, Travel BASIX?: 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 206531

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

FDA NDC Directory listings under ANDA 206531
Product	Strength	Form · route	Labeler	Product NDC
Amazon Basic Care Acid Reducerfamotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-363
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-1899
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-4400
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-5300
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-9607
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Better Living Brands, LLC	21130-033
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Better Living Brands LLC	21130-039
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Amerisource Bergen	46122-735
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Amerisource Bergen	46122-737
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Wal-Mart Stores, Inc.	49035-505
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Wal-Mart Stores, Inc.	49035-589
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Magno-Humphries, Inc.	54257-180
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Magno-Humphries, Inc.	54257-802
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Fred's, Inc.	55315-435
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Family Dollar Stores, LLC	55319-057
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-705
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-706
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-828
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-829
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-859

Showing 20 of 39.

Zantac 360, Travel BASIX (Famotidine tablet, film-coated) NDC 66715-6458