acid relief (famotidine) NDC 11822-1194

Product information

Brand name (proprietary)

acid relief

Generic name (nonproprietary)

famotidine

Active ingredients

Famotidine — 20 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Rite Aid Corporation

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077351

Marketing start

Mar 15, 2023

Marketing end

Dec 31, 2026

Other FDA classes

Histamine H2 Receptor Antagonists (Mechanism)

Identifiers

Product ID 11822-1194_57af3698-0335-483a-a150-29e6b6468284SPL ID 57af3698-0335-483a-a150-29e6b6468284SPL set ID 45789b7a-e9c7-4813-b07b-f88d9108455dRxCUI 310273UNII 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

N411822119401 followed by a unit qualifier and the quantity Copy

Package 11822-1194-01. 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 077351

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

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