What is NDC 72559-032?

72559-032 is the product NDC for Curist Acid Relief (famotidine 20 mg), Famotidine 20 mg/1 tablet, listed with the FDA by Little Pharma, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Curist Acid Relief (Famotidine 20 mg).

Little Pharma, Inc., NDC labeler code 72559. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Curist Acid Relief?

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.

Curist Acid Relief NDC 72559-032 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72559-032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72559-0032Add 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
72559-032-22	7255900322272559003222	200 TABLET in 1 BOTTLE (72559-032-22)Marketed from Aug 15, 2026
72559-032-23	7255900322372559003223	300 TABLET in 1 BOTTLE (72559-032-23)Marketed from Jan 31, 2024
72559-032-63	7255900326372559003263	500 TABLET in 1 BOTTLE (72559-032-63)Marketed from Aug 15, 2026

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): Curist Acid Relief
Generic name (nonproprietary): famotidine 20 mg
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Little Pharma, Inc.NDC labeler code 72559
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215822
Marketing start: Jan 31, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72559-032_56c07eb7-07fe-00c1-e063-6394a90aa202SPL ID 56c07eb7-07fe-00c1-e063-6394a90aa202SPL set ID 0fdfcc7c-aeed-6bd0-e063-6394a90ae52dRxCUI 310273UNII 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

N472559003222 followed by a unit qualifier and the quantity

Package 72559-0032-22. 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 Jul 16, 2026.

Indications (excerpt from the label)

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 food and beverages

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72559-032

What is NDC 72559-032?: 72559-032 is the product NDC for Curist Acid Relief (famotidine 20 mg), Famotidine 20 mg/1 tablet, listed with the FDA by Little Pharma, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Curist Acid Relief (Famotidine 20 mg).
What is the active ingredient?: Famotidine.
Who is the labeler?: Little Pharma, Inc., NDC labeler code 72559. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Curist Acid Relief?: 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 215822

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

FDA NDC Directory listings under ANDA 215822
Product	Strength	Form · route	Labeler	Product NDC
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	VKT Pharma Private Limited	71821-012
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	VKT Pharma Private Limited	71821-012
Heartburn Relieffamotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Shield Pharmaceuticals Corp	83059-0005
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	TWIN MED LLC	55681-342
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	TWIN MED LLC	55681-343
Heartburn Relieffamotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Shield Pharmaceuticals Corp	83059-0185
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	GLENMARK THERAPEUTICS INC., USA	72657-112
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	GLENMARK THERAPEUTICS INC., USA	72657-113
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	FAMILY DOLLAR	55319-408
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	FAMILY DOLLAR	55319-409
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	GLENMARK THERAPEUTICS INC., USA	72657-132
Famotidine	Famotidine 10 mg/1	TabletOral	Bi-Mart	37835-161
Famotidine	Famotidine 20 mg/1	TabletOral	Bi-Mart	37835-165
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	GERI-CARE PHARMACEUTICAL CORP	57896-317
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Geri-Care Pharmaceutical Corp	57896-319
Acid Reducer Maximum Strengthfamotidine 20mg	Famotidine 20 mg/1	TabletOral	Grocery Outlet	85828-443
Welmate Famotidine 20mgfamotidine 20mg	Famotidine 20 mg/1	TabletOral	YYBA Corp	73581-109
Welmate Famotidine 10mgfamotidine 10mg	Famotidine 10 mg/1	TabletOral	YYBA Corp	73581-108
Famotidine	Famotidine 20 mg/1	TabletOral	SAFEWAY	21130-191
Acid Reducer	Famotidine 20 mg/1	TabletOral	Demoulas Super Markets, Inc.	53942-443

Showing 20 of 23.

Curist Acid Relief (Famotidine 20 mg) NDC 72559-032