Cephalexin NDC 63629-9204

Product information

Brand name (proprietary)

Cephalexin

Generic name (nonproprietary)

cephalexin

Active ingredients

Cephalexin — 125 mg/5mL

Dosage form

For suspension

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 210221

Marketing start

Mar 28, 2019

Listing expires

Dec 31, 2026

Other FDA classes

Cephalosporins (Chemical structure)

Identifiers

Product ID 63629-9204_b7e7ec11-dee5-4ed2-ad3d-be967d311e26SPL ID b7e7ec11-dee5-4ed2-ad3d-be967d311e26SPL set ID f4ced8c7-a276-4a44-a60c-f8d1689a2bdfRxCUI 309110UNII OBN7UDS42Y

Pharmacologic class

Cephalosporin 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

N463629920401 followed by a unit qualifier and the quantity Copy

Package 63629-9204-01. 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 210221

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