NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8558Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8558Add 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
0615-8558-050061585580515 TABLET in 1 BLISTER PACK (0615-8558-05)Marketed from Jan 16, 2025
0615-8558-280061585582828 TABLET in 1 BLISTER PACK (0615-8558-28)Marketed from Jan 16, 2025
0615-8558-390061585583930 TABLET in 1 BLISTER PACK (0615-8558-39)Marketed from Jan 16, 2025

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Famotidine
Generic name (nonproprietary)
famotidine
Active ingredients
Famotidine — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078916
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0615-8558_20739b19-9f06-4e88-962e-d812086fdc90SPL ID 20739b19-9f06-4e88-962e-d812086fdc90SPL set ID 59b17677-d805-4d9e-9c64-96385ae47bffRxCUI 284245, 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

N400615855805 followed by a unit qualifier and the quantity

Package 00615-8558-05. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 078916

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

FDA NDC Directory listings under ANDA 078916
ProductStrengthForm · routeLabelerProduct NDC
FamotidineFamotidine 20 mg/1TabletOralBryant Ranch Prepack71335-0409
FamotidineFamotidine 20 mg/1TabletOraldirect rx72189-141
FamotidineFamotidine 20 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3201
FamotidineFamotidine 20 mg/1TabletOralProficient Rx LP63187-723
FamotidineFamotidine 20 mg/1TabletOralAlembic Pharmaceuticals Limited46708-293
FamotidineFamotidine 40 mg/1TabletOralAlembic Pharmaceuticals Limited46708-294
FamotidineFamotidine 20 mg/1TabletOralNorthwind Health Company, LLC82868-077
FamotidineFamotidine 20 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-001
FamotidineFamotidine 40 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-002
FamotidineFamotidine 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4119
FamotidineFamotidine 20 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-399
FamotidineFamotidine 40 mg/1TabletOralProficient Rx LP63187-908
FamotidineFamotidine 40 mg/1TabletOralBryant Ranch Prepack71335-0231
FamotidineFamotidine 40 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8559

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