Amoxicillin NDC 50090-0404

Product information

Brand name (proprietary)

Amoxicillin

Generic name (nonproprietary)

amoxicillin

Active ingredients

Amoxicillin — 125 mg/5mL

Dosage form

Powder, For suspension

Route

Oral

Labeler

A-S Medication Solutions

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 065322

Marketing start

Jun 19, 2006

Listing expires

Dec 31, 2027

Other FDA classes

Penicillins (Chemical structure)

Identifiers

Product ID 50090-0404_712374d0-76de-47f2-b26c-df9d82bbb663SPL ID 712374d0-76de-47f2-b26c-df9d82bbb663SPL set ID 60c7ae87-9631-4b29-9ca4-82fb3bafcab8RxCUI 313797UNII 804826J2HU

Pharmacologic class

Penicillin-class Antibacterial

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

N450090040400 followed by a unit qualifier and the quantity Copy

Package 50090-0404-00. 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

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

Other NDCs under ANDA 065322

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