NDC codes

FDA NDC Directory
Product NDC (as listed)69168-443Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69168-0443Add 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
69168-443-096916804430910 TABLET in 1 BLISTER PACK (69168-443-09)Marketed from Feb 29, 2024
69168-443-3269168044332100 TABLET in 1 BOTTLE (69168-443-32)Marketed from Jan 15, 2024
69168-443-50691680443501 BOTTLE in 1 CARTON (69168-443-50) / 50 TABLET in 1 BOTTLEMarketed from Mar 5, 2024
69168-443-5269168044352225 TABLET in 1 BOTTLE (69168-443-52)Marketed from Jan 15, 2024
69168-443-9969168044399365 TABLET in 1 BOTTLE (69168-443-99)Marketed from Oct 28, 2024

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
Route
Oral
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 69168-443_10efebb0-5d63-4c46-8934-9e91b213a543SPL ID 10efebb0-5d63-4c46-8934-9e91b213a543SPL set ID adc2721d-2ca7-4a47-bae1-be298fa1c155RxCUI 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

N469168044309 followed by a unit qualifier and the quantity

Package 69168-0443-09. 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)

Use(s) 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)

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/1TabletOralBi-Mart37835-161
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-012
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-010
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-010
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-012
FamotidineFamotidine 20 mg/1TabletOralBi-Mart37835-165
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/1TabletOralSAFEWAY21130-191
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralTWIN MED LLC55681-342
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralTWIN MED LLC55681-343
Welmate Famotidine 10mgfamotidine 10mgFamotidine 10 mg/1TabletOralYYBA Corp73581-108
Welmate Famotidine 20mgfamotidine 20mgFamotidine 20 mg/1TabletOralYYBA Corp73581-109
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFAMILY DOLLAR55319-409
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralFAMILY DOLLAR55319-408
Acid Reducer Maximum Strengthfamotidine 20mgFamotidine 20 mg/1TabletOralGrocery Outlet85828-443
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralGeri-Care Pharmaceutical Corp57896-319
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralGERI-CARE PHARMACEUTICAL CORP57896-317

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