Package 42291-083-30

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 42291-083-30
Digits Only 4229108330
Product NDC 42291-083
Description

30 TABLET, FILM COATED in 1 BOTTLE (42291-083-30)

Marketing

Marketing Status
Marketed Since 2022-04-11
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": "485b7203-4a64-fbdc-e063-6294a90ac246", "openfda": {"upc": ["0342291083035"], "unii": ["5FD1131I7S"], "rxcui": ["248656", "308460"], "spl_set_id": ["dc633b7d-5154-7e43-e053-2a95a90ad2a6"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (42291-083-03)", "package_ndc": "42291-083-03", "marketing_start_date": "20220411"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42291-083-30)", "package_ndc": "42291-083-30", "marketing_start_date": "20220411"}], "brand_name": "Azithromycin", "product_id": "42291-083_485b7203-4a64-fbdc-e063-6294a90ac246", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "42291-083", "generic_name": "Azithromycin", "labeler_name": "AvKARE", "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": "20220411", "listing_expiration_date": "20271231"}