Over-the-counter drug · ANDA

acid relief (Famotidine) NDC 11822-1194

Famotidine 20 mg/1 · Tablet, Film coated · Oral · Rite Aid Corporation

NDC codes

FDA NDC Directory
Product NDC (as listed)11822-1194Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11822-1194Add 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
11822-1194-1118221194011 BOTTLE in 1 CARTON (11822-1194-1) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 15, 2023
11822-1194-21182211940225 BLISTER PACK in 1 CARTON (11822-1194-2) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Mar 15, 2023
11822-1194-4118221194041 BOTTLE in 1 CARTON (11822-1194-4) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 15, 2023
11822-1194-5118221194052 BOTTLE in 1 CARTON (11822-1194-5) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 4, 2025

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)
acid relief
Generic name (nonproprietary)
famotidine
Active ingredients
Famotidine — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Rite Aid CorporationNDC labeler code 11822
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077351
Marketing start
Marketing end
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 11822-1194_57af3698-0335-483a-a150-29e6b6468284SPL ID 57af3698-0335-483a-a150-29e6b6468284SPL set ID 45789b7a-e9c7-4813-b07b-f88d9108455dRxCUI 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

N411822119401 followed by a unit qualifier and the quantity

Package 11822-1194-01. 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)

About NDC 11822-1194

What is NDC 11822-1194?
11822-1194 is the product NDC for acid relief (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Rite Aid Corporation. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
acid relief (Famotidine).
What is the active ingredient?
Famotidine.
Who is the labeler?
Rite Aid Corporation, NDC labeler code 11822. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for acid relief?
1 other product NDC are listed under this name. See all acid relief NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other acid relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRite Aid Corporation11822-612311822-6123-00

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
heartburn relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralMeijer Distribution Inc41250-712
equaline heartburn preventionfamotidineFamotidine 20 mg/1Tablet, Film coatedOralUnited Natural Foods, Inc. dba UNFI41163-001
Major Heartburn Relief Maximum StrengthfamotidineFamotidine 20 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-5780
topcare acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralTopco Associates LLC76162-300
careone acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRetail Business Services, LLC72476-150
Rugby FamotidinefamotidineFamotidine 20 mg/1Tablet, Film coatedOralRugby Laboratories0536-1298
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralWalgreen Company0363-1203
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCVS Pharmacy59779-194
careone acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRetail Business Services, LLC72476-299
kirkland signature acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCostco Wholesale Company63981-194
foster and thrive acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralStrategic Sourcing Services LLC70677-1101
CareOne Acid RelieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmerican Sales Company41520-707
Equate FamotidinefamotidineFamotidine 20 mg/1Tablet, Film coatedOralWal-Mart Stores Inc49035-650
Acid ControllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralWalgreen Company0363-0701
Acid ControllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B59640-001
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-088
acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B59640-023
equate famotidinefamotidineFamotidine 20 mg/1Tablet, Film coatedOralWALMART INC.79903-115
Leader Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCardinal Health 110, LLC. dba Leader70000-0654
maximum strengthfamotidineFamotidine 20 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-194

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