Amoxicillin NDC 68788-9948

Product information

Brand name (proprietary)

Amoxicillin

Generic name (nonproprietary)

amoxicillin

Active ingredients

Amoxicillin — 250 mg/5mL

Dosage form

Powder, For suspension

Route

Oral

Labeler

Preferred Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 065387

Marketing start

Jan 12, 2012

Listing expires

Dec 31, 2027

Other FDA classes

Penicillins (Chemical structure)

Identifiers

Product ID 68788-9948_1f544b8d-2ee6-4dc8-8289-9684aaa95119SPL ID 1f544b8d-2ee6-4dc8-8289-9684aaa95119SPL set ID 88e76bdd-39f2-48c4-91ca-609511afd382RxCUI 239191, 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

N468788994801 followed by a unit qualifier and the quantity Copy

Package 68788-9948-01. 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 065387

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