NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7180Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7180Add 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
50090-7180-05009071800090 TABLET, FILM COATED in 1 BOTTLE (50090-7180-0)Marketed from May 30, 2024

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)
Famotidine
Generic name (nonproprietary)
famotidine
Active ingredients
Famotidine — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription 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 50090-7180_c87aa6df-b23d-4398-b904-bcf303f22eebSPL ID c87aa6df-b23d-4398-b904-bcf303f22eebSPL set ID 75a334ee-48b9-47e7-8225-6e595bed8a74RxCUI 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

N450090718000 followed by a unit qualifier and the quantity

Package 50090-7180-00. 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)

Famotidine tablets are indicated in adult and pediatric patients 40 kg and greater for the treatment of: • active duodenal ulcer (DU). • active gastric ulcer (GU). • symptomatic nonerosive gastroesophageal reflux disease (GERD). • erosive esophagitis due to GERD, diagnosed by biopsy. Famotidine tablets are indicated in adults for the: • treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome, multiple endocrine neoplasias). • reduction of the risk of duodenal ulcer recurrence. Famotidine tablets are a histamine-2 (H 2 ) receptor antagonist indicated ( 1 ): In adult and pediatric patients 40 kg and greater for the treatment of: • active duodenal ulcer (DU). • act…

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
Acid ReducerfamotidineFamotidine 20 mg/1TabletOralAllegiant Health69168-445
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7178
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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