heartburn relief (famotidine) NDC 41250-493

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

Meijer Distribution Inc

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075400

Marketing start

Apr 17, 2019

Listing expires

Dec 31, 2026

Other FDA classes

Histamine H2 Receptor Antagonists (Mechanism)

Identifiers

Product ID 41250-493_b7a57732-f641-4f06-aff4-7ee6a96b3025SPL ID b7a57732-f641-4f06-aff4-7ee6a96b3025SPL set ID 05c03fd8-abc8-47f7-868c-895b9a38c5b3RxCUI 199047UNII 5QZO15J2Z8

Pharmacologic class

Histamine-2 Receptor Antagonist

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

N441250049365 followed by a unit qualifier and the quantity Copy

Package 41250-0493-65. 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

Other NDCs under ANDA 075400

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