What is NDC 41226-719?

41226-719 is the product NDC for Original strength heartburn prevention, Famotidine 10 mg/1 tablet, listed with the FDA by KROGER COMPANY. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Original strength heartburn prevention (Famotidine).

KROGER COMPANY, NDC labeler code 41226. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Original strength heartburn prevention?

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.

Original strength heartburn prevention NDC 41226-719

NDC codes

FDA NDC Directory

Product NDC (as listed)41226-719Labeler and product segments. Claims need a package NDC.

Product NDC at billing width41226-0719Add 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
41226-719-06	4122607190641226071906	3 BLISTER PACK in 1 CARTON (41226-719-06) / 10 TABLET in 1 BLISTER PACKMarketed from May 5, 2023
41226-719-09	4122607190941226071909	1 BOTTLE in 1 CARTON (41226-719-09) / 90 TABLET in 1 BOTTLEMarketed from Apr 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): Original strength heartburn prevention
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: KROGER COMPANYNDC labeler code 41226
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217543
Marketing start: May 5, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 41226-719_1cb86ee4-41c1-1196-e063-6394a90a9199SPL ID 1cb86ee4-41c1-1196-e063-6394a90a9199SPL set ID ea1c2838-acbd-18e0-e053-2a95a90a3522RxCUI 199047UNII 5QZO15J2Z8UPC 0041260018459
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

N441226071906 followed by a unit qualifier and the quantity

Package 41226-0719-06. 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 8, 2024.

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 41226-719

What is NDC 41226-719?: 41226-719 is the product NDC for Original strength heartburn prevention, Famotidine 10 mg/1 tablet, listed with the FDA by KROGER COMPANY. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Original strength heartburn prevention (Famotidine).
What is the active ingredient?: Famotidine.
Who is the labeler?: KROGER COMPANY, NDC labeler code 41226. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Original strength heartburn prevention?: 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 217543

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

FDA NDC Directory listings under ANDA 217543
Product	Strength	Form · route	Labeler	Product NDC
Famotidine 10 mg	Famotidine 10 mg/1	Tablet, CoatedOral	MARKSANS PHARMA LIMITED	25000-086
Famotidine 20 mg	Famotidine 20 mg/1	Tablet, CoatedOral	MARKSANS PHARMA LIMITED	25000-087
Famotidine 20 mg	Famotidine 20 mg/1	Tablet, CoatedOral	MARKSANS PHARMA LIMITED	25000-124
Maximum Strength Acid Controllerfamotidine	Famotidine 20 mg/1	TabletOral	BETTER LIVING BRANDS LLC.	21130-027
Maximum Strength Acid Reducerfamotidine	Famotidine 20 mg/1	TabletOral	TARGET CORPORATION	11673-697
Maximum Strength Acid Reducerfamotidine	Famotidine 20 mg/1	TabletOral	TIME CAP LABORATORIES,INC	49483-720

Original strength heartburn prevention (Famotidine) NDC 41226-719