What is NDC 82725-4047?

82725-4047 is the product NDC for Goodmeds Famotidine 20mg 500 count, Famotidine 20 mg/1 tablet, listed with the FDA by Cabinet Health P.B.C.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Goodmeds Famotidine 20mg 500 count (Famotidine 20mg).

Cabinet Health P.B.C., NDC labeler code 82725. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Goodmeds Famotidine 20mg 500 count?

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.

Goodmeds Famotidine 20mg 500 count NDC 82725-4047

NDC codes

FDA NDC Directory

Product NDC (as listed)82725-4047Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82725-4047Add 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
82725-4047-1	8272540470182725404701	500 TABLET in 1 BOTTLE (82725-4047-1)Marketed from Jul 3, 2026

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): Goodmeds Famotidine 20mg 500 count
Generic name (nonproprietary): famotidine 20mg
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Cabinet Health P.B.C.NDC labeler code 82725
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215766
Marketing start: Jul 3, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 82725-4047_5592d0f0-03fe-c914-e063-6294a90a2826SPL ID 5592d0f0-03fe-c914-e063-6294a90a2826SPL set ID 5592d0f0-03fd-c914-e063-6294a90a2826RxCUI 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

N482725404701 followed by a unit qualifier and the quantity

Package 82725-4047-01. 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 1, 2026.

Indications (excerpt from the label)

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 82725-4047

What is NDC 82725-4047?: 82725-4047 is the product NDC for Goodmeds Famotidine 20mg 500 count, Famotidine 20 mg/1 tablet, listed with the FDA by Cabinet Health P.B.C.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Goodmeds Famotidine 20mg 500 count (Famotidine 20mg).
What is the active ingredient?: Famotidine.
Who is the labeler?: Cabinet Health P.B.C., NDC labeler code 82725. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Goodmeds Famotidine 20mg 500 count?: 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 215766

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

FDA NDC Directory listings under ANDA 215766
Product	Strength	Form · route	Labeler	Product NDC
famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Camber Consumer Care Inc	69230-326
Famotidine	Famotidine 10 mg/10mg	TabletOral	Little Pharma, Inc.	72559-038
famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-003
famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-008
Heartburn Relieffamotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Shield Pharmaceuticals Corp	83059-0031

Goodmeds Famotidine 20mg 500 count (Famotidine 20mg) NDC 82725-4047