What is NDC 41167-0364?

41167-0364 is the product NDC for Zantac 360 Cool Mint (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Chattem, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Zantac 360 Cool Mint (Famotidine).

Chattem, Inc., NDC labeler code 41167. 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 Cool Mint?

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 Cool Mint NDC 41167-0364

NDC codes

FDA NDC Directory

Product NDC (as listed)41167-0364Labeler and product segments. Claims need a package NDC.

Product NDC at billing width41167-0364Add 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
41167-0364-0	4116703640041167036400	1 BOTTLE in 1 CARTON (41167-0364-0) / 25 TABLET, FILM COATED in 1 BOTTLEMarketed from Dec 1, 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 Cool Mint
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Chattem, Inc.NDC labeler code 41167
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206531
Marketing start: Dec 1, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 41167-0364_a185b361-cf81-4912-8020-d8f778903597SPL ID a185b361-cf81-4912-8020-d8f778903597SPL set ID 19fe7c6e-243c-4005-a63a-f8cac1ce55c8RxCUI 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

N441167036400 followed by a unit qualifier and the quantity

Package 41167-0364-00. 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 Sep 30, 2025.

Indications (excerpt from the label)

Use s ■ 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 food and beverages

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 41167-0364

What is NDC 41167-0364?: 41167-0364 is the product NDC for Zantac 360 Cool Mint (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Chattem, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Zantac 360 Cool Mint (Famotidine).
What is the active ingredient?: Famotidine.
Who is the labeler?: Chattem, Inc., NDC labeler code 41167. 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 Cool Mint?: 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 Cool Mint (Famotidine) NDC 41167-0364