Over-the-counter drug · ANDA

Heartburn Relief (Famotidine) NDC 83059-0185

Famotidine 10 mg/1 · Tablet, Film coated · Oral · Shield Pharmaceuticals Corp

NDC codes

FDA NDC Directory
Product NDC (as listed)83059-0185Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83059-0185Add 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
83059-0185-1830590185011 BOTTLE in 1 CARTON (83059-0185-1) / 15 TABLET, FILM COATED in 1 BOTTLEMarketed from Sep 24, 2026

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)
Heartburn Relief
Generic name (nonproprietary)
famotidine
Active ingredients
Famotidine — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Shield Pharmaceuticals CorpNDC labeler code 83059
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 83059-0185_5c3f7648-b027-9de5-e063-6394a90a7b6bSPL ID 5c3f7648-b027-9de5-e063-6394a90a7b6b

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

N483059018501 followed by a unit qualifier and the quantity

Package 83059-0185-01. 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

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

About NDC 83059-0185

What is NDC 83059-0185?
83059-0185 is the product NDC for Heartburn Relief (famotidine), Famotidine 10 mg/1 tablet, film coated, listed with the FDA by Shield Pharmaceuticals Corp. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Heartburn Relief (Famotidine).
What is the active ingredient?
Famotidine.
Who is the labeler?
Shield Pharmaceuticals Corp, NDC labeler code 83059. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Heartburn Relief?
8 other product NDCs are listed under this name. See all Heartburn 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 Heartburn Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Heartburn Reliefaluminum hydroxide and magnesium carbonateAluminum hydroxide 254 mg/5mL; Magnesium carbonate 237.5 mg/5mLSuspensionOralGERI-CARE PHARMACEUTICALS, CORP57896-56557896-0565-12
Heartburn RelieffamotidineFamotidine 10 mg/1Tablet, Film coatedOralShield Pharmaceuticals Corp83059-003183059-0031-05
Heartburn RelieffamotidineFamotidine 10 mg/1Tablet, Film coatedOralShield Pharmaceuticals Corp83059-000583059-0005-05
Heartburn Reliefaluminum hydroxide and magnesium carbonateAluminum hydroxide 254 mg/5mL; Magnesium carbonate 237.5 mg/5mLSuspensionOralCHAIN DRUG MARKETING ASSOCIATION63868-56563868-0565-12
heartburn relieffamotidineFamotidine 20 mg/1Tablet, Film coatedOralMeijer Distribution Inc41250-71241250-0712-0241250-0712-7141250-0712-78
heartburn relieffamotidineFamotidine 10 mg/1Tablet, Film coatedOralMeijer Distribution Inc41250-49341250-0493-6541250-0493-72
Heartburn Reliefcarbo moreActivated charcoal 6 [hp_X]/1 + 5 more ingredientsTablet, Orally disintegratingOralTRP Company17312-03017312-0030-14
heartburn reliefcimetidineCimetidine 200 mg/1Tablet, Film coatedOralCVS Pharmacy59779-02259779-0022-7259779-0022-76

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 coatedOralGERI-CARE PHARMACEUTICAL CORP57896-317
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGeri-Care Pharmaceutical Corp57896-319
FamotidineFamotidine 10 mg/1TabletOralBi-Mart37835-161
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-010
FamotidineFamotidine 20 mg/1TabletOralBi-Mart37835-165
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-010
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-012
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-012
Acid ReducerfamotidineFamotidine 20 mg/1TabletOralAllegiant Health69168-443
Curist Acid Relieffamotidine 20 mgFamotidine 20 mg/1TabletOralLittle Pharma, Inc.72559-032
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralGLENMARK THERAPEUTICS INC., USA72657-112
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGLENMARK THERAPEUTICS INC., USA72657-113
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGLENMARK THERAPEUTICS INC., USA72657-132
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralTWIN MED LLC55681-342
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralTWIN MED LLC55681-343
Acid Reducer Maximum Strengthfamotidine 20mgFamotidine 20 mg/1TabletOralGrocery Outlet85828-443
FamotidineFamotidine 20 mg/1TabletOralSAFEWAY21130-191
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralFAMILY DOLLAR55319-408
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFAMILY DOLLAR55319-409
Welmate Famotidine 10mgfamotidine 10mgFamotidine 10 mg/1TabletOralYYBA Corp73581-108

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