Package 67296-0020-1
Brand: zithromax
Generic: azithromycin dihydratePackage Facts
Identity
Package NDC
67296-0020-1
Digits Only
6729600201
Product NDC
67296-0020
Description
4 TABLET, FILM COATED in 1 BOTTLE (67296-0020-1)
Marketing
Marketing Status
Brand
zithromax
Generic
azithromycin dihydrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ddecd2f-ea4c-536f-e063-6294a90a7936", "openfda": {"upc": ["0300693060306", "0300693070305"], "unii": ["5FD1131I7S"], "rxcui": ["212446", "308460"], "spl_set_id": ["3ddecd25-dc32-a2af-e063-6294a90a526d"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (67296-0020-1)", "package_ndc": "67296-0020-1", "marketing_start_date": "19960718"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (67296-0020-2)", "package_ndc": "67296-0020-2", "marketing_start_date": "19960718"}], "brand_name": "Zithromax", "product_id": "67296-0020_3ddecd2f-ea4c-536f-e063-6294a90a7936", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "67296-0020", "generic_name": "azithromycin dihydrate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zithromax", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "NDA050711", "marketing_category": "NDA", "marketing_start_date": "19960718", "listing_expiration_date": "20261231"}