Azithromycin Dihydrate NDC 68094-900

Product information

Brand name (proprietary)

Azithromycin Dihydrate

Generic name (nonproprietary)

azithromycin dihydrate

Active ingredients

Azithromycin dihydrate — 250 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Precision Dose, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208250

Marketing start

Feb 15, 2024

Listing expires

Dec 31, 2027

Other FDA classes

Macrolides (Chemical structure)

Identifiers

Product ID 68094-900_1200c2bd-75cb-4855-b24b-b5627726ac2dSPL ID 1200c2bd-75cb-4855-b24b-b5627726ac2dSPL set ID d9b66736-3f1a-4d6d-bdc4-274f5adfb40cRxCUI 308460, 749783UNII 5FD1131I7SUPC 0368094900508

Pharmacologic class

Macrolide Antimicrobial

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

N468094090006 followed by a unit qualifier and the quantity Copy

Package 68094-0900-06. 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 208250

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