NDC codes

FDA NDC Directory
Product NDC (as listed)72288-629Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72288-0629Add 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
72288-629-7872288062978722880629781 BOTTLE in 1 CARTON (72288-629-78) / 100 TABLET, FILM COATED in 1 BOTTLE (72288-629-00)Marketed from Sep 11, 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
Amazon.com Services LLCNDC labeler code 72288
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 72288-629_8da3cb4f-b9c6-4a91-a89c-fb44ecfe150bSPL ID 8da3cb4f-b9c6-4a91-a89c-fb44ecfe150b

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

N472288062978 followed by a unit qualifier and the quantity

Package 72288-0629-78. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 72288-629

What is NDC 72288-629?
72288-629 is the product NDC for Acid Reducer (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Amazon.com Services LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acid Reducer (Famotidine).
What is the active ingredient?
Famotidine.
Who is the labeler?
Amazon.com Services LLC, NDC labeler code 72288. 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 Reducer?
33 other product NDCs are listed under this name. See all Acid Reducer 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 Reducer NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Acid ReducerfamotidineFamotidine 10 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-75672288-0756-75
Acid ReducerfamotidineFamotidine 10 mg/1Tablet, Film coatedOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-81651316-0816-3951316-0816-75
Acid ReducercimetidineCimetidine 200 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-47072288-0470-76
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-51151316-0511-6351316-0511-7151316-0511-78+1 more
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-08856062-0088-02
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralHyVee Inc42507-19442507-0194-0142507-0194-7142507-0194-78
Acid ReducerfamotidineFamotidine 20 mg/1TabletOralAllegiant Health69168-44569168-0445-3269168-0445-52
Acid ReduceromeprazoleOmeprazole magnesium 20 mg/1Tablet, Delayed releaseOralFamily Dollar Stores, LLC55319-03755319-0037-0555319-0037-62
Acid ReducerfamotidineFamotidine 20 mg/1TabletOralAllegiant Health69168-44369168-0443-0969168-0443-3269168-0443-50+2 more
Acid ReduceromeprazoleOmeprazole magnesium 20 mg/1Tablet, Delayed releaseOralINNOVUS PHARMACEUTICALS, INC.57483-12057483-0120-1457483-0120-42

All 34 Acid Reducer NDCs

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
Acid ControllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralWalgreen Company0363-0701
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralWalgreen Company0363-1203
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralSafeway21130-521
Acid ControllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B37808-042
Acid ControllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B59640-001
acid controllerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCVS Pharmacy59779-194
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralHyVee Inc42507-194
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-511
Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-088
acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralH E B59640-023
acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralCVS Pharmacy69842-659
acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRite Aid Corporation11822-1194
acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRite Aid Corporation11822-6123
basic care acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-194
basic care acid reducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-329
basic care heartburn preventionfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-151
berkley and jensen famotidinefamotidineFamotidine 20 mg/1Tablet, Film coatedOralBJWC68391-300
CareOne Acid RelieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmerican Sales Company41520-707
careone acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRetail Business Services, LLC72476-150
careone acid relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralRetail Business Services, LLC72476-299

Showing 20 of 39.

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