Package 71205-430-04
Brand: azithromycin dihydrate
Generic: azithromycin dihydratePackage Facts
Identity
Package NDC
71205-430-04
Digits Only
7120543004
Product NDC
71205-430
Description
4 TABLET, FILM COATED in 1 BOTTLE (71205-430-04)
Marketing
Marketing Status
Brand
azithromycin dihydrate
Generic
azithromycin dihydrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edcedd16-fe45-4edb-a0f8-55d904a59096", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["8037c6f4-4881-4740-8229-2aee56141cd0"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (71205-430-04)", "package_ndc": "71205-430-04", "marketing_start_date": "20201223"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-430-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-430-06", "marketing_start_date": "20200317"}], "brand_name": "Azithromycin Dihydrate", "product_id": "71205-430_edcedd16-fe45-4edb-a0f8-55d904a59096", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-430", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}