Package 70518-2433-2

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 70518-2433-2
Digits Only 7051824332
Product NDC 70518-2433
Description

6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2433-2)

Marketing

Marketing Status
Marketed Since 2020-01-28
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": "4a1920e3-a616-c993-e063-6394a90a824a", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["5f144e92-c9eb-420a-9bb8-4265a9f20a98"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2433-2)", "package_ndc": "70518-2433-2", "marketing_start_date": "20200128"}], "brand_name": "Azithromycin", "product_id": "70518-2433_4a1920e3-a616-c993-e063-6394a90a824a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-2433", "generic_name": "Azithromycin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA207370", "marketing_category": "ANDA", "marketing_start_date": "20191119", "listing_expiration_date": "20271231"}