NDC codes

FDA NDC Directory
Product NDC (as listed)69168-445Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69168-0445Add 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
69168-445-3269168044532100 TABLET in 1 BOTTLE (69168-445-32)Marketed from Oct 31, 2024
69168-445-5269168044552225 TABLET in 1 BOTTLE (69168-445-52)Marketed from Oct 31, 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 215767
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 69168-445_8b9d16df-e73f-45e1-b5f9-3dfaa8c4b5f7SPL ID 8b9d16df-e73f-45e1-b5f9-3dfaa8c4b5f7SPL set ID 5c6c6665-cb0a-41d1-af28-85b4f061bd1bRxCUI 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

N469168044532 followed by a unit qualifier and the quantity

Package 69168-0445-32. 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 215767

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

FDA NDC Directory listings under ANDA 215767
ProductStrengthForm · routeLabelerProduct NDC
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-331
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6790
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-589
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7178
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7180
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7196
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0329
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralRedpharm Drug67296-2264
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-427
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2527
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralST. MARY'S MEDICAL PARK PHARMACY60760-937
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3786
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-017
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-018
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-8733
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralRedpharm Drug67296-2330

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