Package 0069-3070-30

Brand: zithromax

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 0069-3070-30
Digits Only 0069307030
Product NDC 0069-3070
Product ID 0069-3070_e15f2173-8700-4392-96a4-8560772b6f8a
Description

30 TABLET, FILM COATED in 1 BOTTLE (0069-3070-30)

Marketing

Marketing Status
Marketed Since 2002-05-24
Brand zithromax
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Zithromax ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e15f2173-8700-4392-96a4-8560772b6f8a", "openfda": {"upc": ["0300693060306", "0300693070305"], "unii": ["5FD1131I7S"], "rxcui": ["105260", "141963", "211307", "212446", "226827", "248656", "308459", "308460", "749780", "749783", "750149", "750157"], "spl_set_id": ["db52b91e-79f7-4cc1-9564-f2eee8e31c45"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0069-3070-30)", "package_ndc": "0069-3070-30", "marketing_start_date": "20020524"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0069-3070-75)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0069-3070-75", "marketing_start_date": "20020524"}], "brand_name": "Zithromax", "product_id": "0069-3070_e15f2173-8700-4392-96a4-8560772b6f8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0069-3070", "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/1"}], "application_number": "NDA050784", "marketing_category": "NDA", "marketing_start_date": "20020524", "listing_expiration_date": "20271231"}