What is NDC 72288-363?

72288-363 is the product NDC for Amazon Basic Care Acid Reducer (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Amazon.com Services LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Amazon Basic Care Acid Reducer (Famotidine).

Amazon.com Services LLC, NDC labeler code 72288. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Amazon Basic Care Acid Reducer?

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.

Amazon Basic Care Acid Reducer NDC 72288-363

NDC codes

FDA NDC Directory

Product NDC (as listed)72288-363Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72288-0363Add 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
72288-363-14	7228803631472288036314	1 BOTTLE in 1 CARTON (72288-363-14) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024
72288-363-34	7228803633472288036334	1 BOTTLE in 1 CARTON (72288-363-34) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024
72288-363-40	7228803634072288036340	2 BOTTLE in 1 CARTON (72288-363-40) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024
72288-363-53	7228803635372288036353	1 BOTTLE in 1 CARTON (72288-363-53) / 25 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024

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): Amazon Basic Care Acid Reducer
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Amazon.com Services LLCNDC labeler code 72288
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206531
Marketing start: May 15, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72288-363_7d01f9d4-fd00-441d-bc52-c2e9ccdac464SPL ID 7d01f9d4-fd00-441d-bc52-c2e9ccdac464
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

N472288036314 followed by a unit qualifier and the quantity

Package 72288-0363-14. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 72288-363

What is NDC 72288-363?: 72288-363 is the product NDC for Amazon Basic Care Acid Reducer (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Amazon.com Services LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Amazon Basic Care Acid Reducer (Famotidine).
What is the active ingredient?: Famotidine.
Who is the labeler?: Amazon.com Services LLC, NDC labeler code 72288. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Amazon Basic Care Acid Reducer?: 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
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
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Best Choice	63941-009

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Amazon Basic Care Acid Reducer (Famotidine) NDC 72288-363