NDC 0069-3150 – Zithromax

Azithromycin Dihydrate 500 mg/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0069-3150

Product details

Brand name
Zithromax
Generic name
Azithromycin dihydrate
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA050733
Marketed since
January 30, 1997
Listing expires
December 31, 2027
Pharmacologic class
Macrolide Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Zithromax →

Package NDC codes (1)

Package NDCDescriptionSince
0069-3150-8310 VIAL in 1 CARTON (0069-3150-83) / 5 mL in 1 VIAL (0069-3150-84)Jan 30, 1997

Recalls mentioning this NDC

Other Zithromax products