Package 70518-0784-1

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 70518-0784-1
Digits Only 7051807841
Product NDC 70518-0784
Description

4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0784-1)

Marketing

Marketing Status
Marketed Since 2019-12-23
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": "48372a1c-5fe3-bf47-e063-6394a90a43c2", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["308460"], "spl_set_id": ["333ffe63-aaeb-4dff-b595-1c11209189a6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0784-1)", "package_ndc": "70518-0784-1", "marketing_start_date": "20191223"}], "brand_name": "Azithromycin", "product_id": "70518-0784_48372a1c-5fe3-bf47-e063-6394a90a43c2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-0784", "generic_name": "Azithromycin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA065225", "marketing_category": "ANDA", "marketing_start_date": "20171012", "listing_expiration_date": "20271231"}