NDC codes

FDA NDC Directory
Product NDC (as listed)72288-470Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72288-0470Add 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
72288-470-7672288047076722880470761 BOTTLE in 1 CARTON (72288-470-76) / 120 TABLET, FILM COATED in 1 BOTTLE (72288-470-00)Marketed from Jul 30, 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)
cimetidine
Active ingredients
Cimetidine — 200 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 075285
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 72288-470_d7a5b623-2188-4781-aa42-3ecc8ca4eaa9SPL ID d7a5b623-2188-4781-aa42-3ecc8ca4eaa9SPL set ID 81dbc581-aa51-46bf-8b69-6d926de2f583RxCUI 197505UNII 80061L1WGD

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

N472288047076 followed by a unit qualifier and the quantity

Package 72288-0470-76. 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 foods and beverages

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72288-470

What is NDC 72288-470?
72288-470 is the product NDC for Acid Reducer (cimetidine), Cimetidine 200 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 (Cimetidine).
What is the active ingredient?
Cimetidine.
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 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-62972288-0629-78
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 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 075285

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

FDA NDC Directory listings under ANDA 075285
ProductStrengthForm · routeLabelerProduct NDC
Acid ControllercimetidineCimetidine 200 mg/1Tablet, Film coatedOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-739
basic care acid reducercimetidineCimetidine 200 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-022
cimetidine 200 acid reducercimetidineCimetidine 200 mg/1Tablet, Film coatedOralWalgreen Company0363-0022
Equate CimetidinecimetidineCimetidine 200 mg/1Tablet, Film coatedOralWal-Mart Stores Inc49035-820
heartburn preventioncimetidineCimetidine 200 mg/1Tablet, Film coatedOralH E B59640-022
heartburn reliefcimetidineCimetidine 200 mg/1Tablet, Film coatedOralCVS Pharmacy59779-022

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