Package 71205-503-03

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 71205-503-03
Digits Only 7120550303
Product NDC 71205-503
Description

1 BLISTER PACK in 1 BAG (71205-503-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-02-26
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31df881c-4b9b-4717-8f76-98b6ca8be644", "openfda": {"upc": ["0371205503031"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["34e6364a-ac3d-434e-a90c-cb13ebcf7983"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BAG (71205-503-03)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-503-03", "marketing_start_date": "20210226"}], "brand_name": "Azithromycin", "product_id": "71205-503_31df881c-4b9b-4717-8f76-98b6ca8be644", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-503", "generic_name": "Azithromycin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA210001", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}