Maximum Strength Acid Reducer (famotidine) NDC 11673-697

NDC codes

FDA NDC Directory

Product NDC (as listed)11673-697Labeler and product segments. Claims need a package NDC.

Product NDC at billing width11673-0697Add 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
11673-697-01	11673069701	2 BOTTLE in 1 CARTON (11673-697-01) / 50 TABLET in 1 BOTTLEMarketed from May 15, 2024
11673-697-05	11673069705	1 BOTTLE in 1 CARTON (11673-697-05) / 50 TABLET in 1 BOTTLEMarketed from May 15, 2024
11673-697-20	11673069720	1 BOTTLE in 1 CARTON (11673-697-20) / 200 TABLET in 1 BOTTLEMarketed from May 15, 2024
11673-697-52	11673069752	5 BLISTER PACK in 1 CARTON (11673-697-52) / 5 TABLET in 1 BLISTER PACKMarketed 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): Maximum Strength Acid Reducer
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: TARGET CORPORATION
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217543
Marketing start: May 15, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 11673-697_18567eaf-6b97-8c6f-e063-6294a90a986dSPL ID 18567eaf-6b97-8c6f-e063-6294a90a986dSPL set ID 07a924f1-14cc-4e7d-e063-6394a90ac7f3RxCUI 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

N411673069701 followed by a unit qualifier and the quantity

Package 11673-0697-01. 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 May 13, 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)

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
Original strength heartburn preventionfamotidine	Famotidine 10 mg/1	TabletOral	KROGER COMPANY	41226-719
Maximum Strength Acid Reducerfamotidine	Famotidine 20 mg/1	TabletOral	TIME CAP LABORATORIES,INC	49483-720
Maximum Strength Acid Controllerfamotidine	Famotidine 20 mg/1	TabletOral	BETTER LIVING BRANDS LLC.	21130-027
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