Package 0069-3150-83

Brand: zithromax

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 0069-3150-83
Digits Only 0069315083
Product NDC 0069-3150
Description

10 VIAL in 1 CARTON (0069-3150-83) / 5 mL in 1 VIAL (0069-3150-84)

Marketing

Marketing Status
Marketed Since 1997-01-30
Brand zithromax
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b0eb7eb4-90fe-4add-a327-e8be68165a3b", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["1668238", "1668240"], "spl_set_id": ["3b631aa1-2d46-40bc-a614-d698301ea4f9"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0069-3150-83)  / 5 mL in 1 VIAL (0069-3150-84)", "package_ndc": "0069-3150-83", "marketing_start_date": "19970130"}], "brand_name": "Zithromax", "product_id": "0069-3150_b0eb7eb4-90fe-4add-a327-e8be68165a3b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0069-3150", "generic_name": "azithromycin dihydrate", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zithromax", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/5mL"}], "application_number": "NDA050733", "marketing_category": "NDA", "marketing_start_date": "19970130", "listing_expiration_date": "20261231"}