Cefdinir NDC 65862-219

Product information

Brand name (proprietary)

Cefdinir

Generic name (nonproprietary)

cefdinir

Active ingredients

Cefdinir — 250 mg/5mL

Dosage form

Powder, For suspension

Route

Oral

Labeler

Aurobindo Pharma Limited

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 065473

Marketing start

Dec 14, 2007

Listing expires

Dec 31, 2026

Other FDA classes

Cephalosporins (Chemical structure)

Identifiers

Product ID 65862-219_9cfbe4a1-045c-489f-8ca7-9d595997dab7SPL ID 9cfbe4a1-045c-489f-8ca7-9d595997dab7SPL set ID 06fbdb63-d32f-4212-9962-f1de15597ddaRxCUI 309054, 476576UNII CI0FAO63WC

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

N465862021901 followed by a unit qualifier and the quantity Copy

Package 65862-0219-01. 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 065473

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