Over-the-counter drug · ANDA

Acid Reducer (famotidine) NDC 42507-194

Famotidine 20 mg/1 · Tablet, Film coated · Oral · HyVee Inc

NDC codes

FDA NDC Directory
Product NDC (as listed)42507-194Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42507-0194Add 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 NDC11-digit (billing)PackageCopy
42507-194-014250701940125 BLISTER PACK in 1 CARTON (42507-194-01) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Feb 25, 2026
42507-194-71425070194711 BOTTLE in 1 CARTON (42507-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE (42507-194-50)Marketed from Feb 25, 2026
42507-194-78425070194781 BOTTLE in 1 CARTON (42507-194-78) / 100 TABLET, FILM COATED in 1 BOTTLE (42507-194-00)Marketed from Mar 18, 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)
Acid Reducer
Generic name (nonproprietary)
famotidine
Active ingredients
Famotidine — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
HyVee Inc
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077351
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 42507-194_ad62930b-1add-4138-b290-5174d04508e1SPL ID ad62930b-1add-4138-b290-5174d04508e1SPL set ID 381db08e-5756-4255-8202-1d8e6a1cf038RxCUI 310273UNII 5QZO15J2Z8

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

N442507019401 followed by a unit qualifier and the quantity

Package 42507-0194-01. 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 .

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 077351

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

FDA NDC Directory listings under ANDA 077351
ProductStrengthForm · routeLabelerProduct NDC
equaline heartburn preventionfamotidineFamotidine 20 mg/1Tablet, Film coatedOralUnited Natural Foods, Inc. dba UNFI41163-001
careone acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRetail Business Services, LLC72476-150
heartburn relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralMeijer Distribution Inc41250-712
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralSafeway21130-521
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCVS Pharmacy59779-194
CareOne Acid RelieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmerican Sales Company41520-707
Equate FamotidinefamotidineFamotidine 20 mg/1Tablet, Film coatedOralWal-Mart Stores Inc49035-650
kirkland signature acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCostco Wholesale Company63981-194
Good Sense Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralL. Perrigo Company0113-0194
Acid ControllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B59640-001
acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B59640-023
Rugby FamotidinefamotidineFamotidine 20 mg/1Tablet, Film coatedOralRugby Laboratories0536-1298
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-088
foster and thrive acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralStrategic Sourcing Services LLC70677-1101
topcare acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralTopco Associates LLC76162-300
basic care heartburn preventionfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-151
heartburn preventionfamotidineFamotidine 20 mg/1Tablet, Film coatedOralKroger Company30142-194
basic care acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-194
maximum strengthfamotidineFamotidine 20 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-194
acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRite Aid Corporation11822-6123

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