NDC codes

FDA NDC Directory
Product NDC (as listed)53942-443Labeler and product segments. Claims need a package NDC.
Product NDC at billing width53942-0443Add 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
53942-443-2553942044325539420443251 BOTTLE in 1 CARTON (53942-443-25) / 25 TABLET in 1 BOTTLEMarketed from Nov 30, 2023
53942-443-5053942044350539420443501 BOTTLE in 1 CARTON (53942-443-50) / 50 TABLET in 1 BOTTLEMarketed from Nov 30, 2023

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)
acid reducer
Active ingredients
Famotidine — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Demoulas Super Markets, Inc.NDC labeler code 53942
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215822
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 53942-443_b53bbe14-3a58-4212-8f9d-46be5f48fdc6SPL ID b53bbe14-3a58-4212-8f9d-46be5f48fdc6

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

N453942044325 followed by a unit qualifier and the quantity

Package 53942-0443-25. 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 53942-443

What is NDC 53942-443?
53942-443 is the product NDC for Acid Reducer, Famotidine 20 mg/1 tablet, listed with the FDA by Demoulas Super Markets, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acid Reducer.
What is the active ingredient?
Famotidine.
Who is the labeler?
Demoulas Super Markets, Inc., NDC labeler code 53942. 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 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

All 34 Acid Reducer NDCs

Other NDCs under ANDA 215822

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

FDA NDC Directory listings under ANDA 215822
ProductStrengthForm · routeLabelerProduct NDC
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-012
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-012
Heartburn RelieffamotidineFamotidine 10 mg/1Tablet, Film coatedOralShield Pharmaceuticals Corp83059-0005
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralTWIN MED LLC55681-342
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralTWIN MED LLC55681-343
Curist Acid Relieffamotidine 20 mgFamotidine 20 mg/1TabletOralLittle Pharma, Inc.72559-032
Heartburn RelieffamotidineFamotidine 10 mg/1Tablet, Film coatedOralShield Pharmaceuticals Corp83059-0185
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralGLENMARK THERAPEUTICS INC., USA72657-112
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGLENMARK THERAPEUTICS INC., USA72657-113
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralFAMILY DOLLAR55319-408
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFAMILY DOLLAR55319-409
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGLENMARK THERAPEUTICS INC., USA72657-132
FamotidineFamotidine 10 mg/1TabletOralBi-Mart37835-161
FamotidineFamotidine 20 mg/1TabletOralBi-Mart37835-165
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralGERI-CARE PHARMACEUTICAL CORP57896-317
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGeri-Care Pharmaceutical Corp57896-319
Acid Reducer Maximum Strengthfamotidine 20mgFamotidine 20 mg/1TabletOralGrocery Outlet85828-443
Welmate Famotidine 20mgfamotidine 20mgFamotidine 20 mg/1TabletOralYYBA Corp73581-109
Welmate Famotidine 10mgfamotidine 10mgFamotidine 10 mg/1TabletOralYYBA Corp73581-108
FamotidineFamotidine 20 mg/1TabletOralSAFEWAY21130-191

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