Over-the-counter drug · ANDA

Zantac 360 (Famotidine tablet, film-coated) NDC 66715-9758

Famotidine 20 mg/1 · Tablet, Film coated · Oral · Lil' Drug Store Products, Inc

NDC codes

FDA NDC Directory
Product NDC (as listed)66715-9758Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66715-9758Add 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 NDC11-digit (billing)PackageCopy
66715-9758-266715975802667159758021 BLISTER PACK in 1 CARTON (66715-9758-2) / 2 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jan 5, 2023
66715-9758-566715975805667159758051 BLISTER PACK in 1 CARTON (66715-9758-5) / 5 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Sep 20, 2021

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
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
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 66715-9758_274bc24b-823e-516d-e063-6394a90a2680SPL ID 274bc24b-823e-516d-e063-6394a90a2680SPL set ID ea38535a-c9db-d03f-e053-2a95a90adf2dRxCUI 310273, 2609246UNII 5QZO15J2Z8

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

N466715975802 followed by a unit qualifier and the quantity

Package 66715-9758-02. 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 .

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 66715-9758

What is NDC 66715-9758?
66715-9758 is the product NDC for Zantac 360, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Lil' Drug Store Products, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Zantac 360 (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?
3 other product NDCs are listed under this name. See all Zantac 360 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 Zantac 360 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Zantac 360famotidineFamotidine 20 mg/1Tablet, Film coatedOralNavajo Manufacturing Company Inc.67751-21467751-0214-0167751-0214-02
Zantac 360famotidineFamotidine 20 mg/1Tablet, Film coatedOralChattem, Inc.41167-036141167-0361-0041167-0361-0141167-0361-02+4 more
Zantac 360famotidineFamotidine 20 mg/1Tablet, Film coatedOralSelect Consumer Group LLC85237-192685237-1926-0185237-1926-02

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
ProductStrengthForm · routeLabelerProduct NDC
Amazon Basic Care Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-363
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralWALGREEN CO.0363-1899
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralWALGREEN CO.0363-4400
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralWALGREEN CO.0363-5300
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralWALGREEN CO.0363-9607
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralBetter Living Brands, LLC21130-033
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralBetter Living Brands LLC21130-039
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralAmerisource Bergen46122-735
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmerisource Bergen46122-737
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralWal-Mart Stores, Inc.49035-505
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralWal-Mart Stores, Inc.49035-589
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralMagno-Humphries, Inc.54257-180
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralMagno-Humphries, Inc.54257-802
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFred's, Inc.55315-435
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFamily Dollar Stores, LLC55319-057
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralAurohealth LLC58602-705
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAurohealth LLC58602-706
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralAurohealth LLC58602-828
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAurohealth LLC58602-829
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAurohealth LLC58602-859

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