Package 70518-3501-3

Brand: Azithromycin Dihydrate

Generic: Azithromycin Dihydrate
NDC Package

Package Facts

Identity

Package NDC 70518-3501-3
Digits Only 7051835013
Product NDC 70518-3501
Description

6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3501-3)

Marketing

Marketing Status
Discontinued 2026-11-30
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": "3aade28f-99db-4196-e063-6294a90a61f7", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["efa7b126-71d2-43be-b3dc-32536217d308"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3501-3)", "package_ndc": "70518-3501-3", "marketing_end_date": "20261130", "marketing_start_date": "20231018"}], "brand_name": "Azithromycin Dihydrate", "product_id": "70518-3501_3aade28f-99db-4196-e063-6294a90a61f7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-3501", "generic_name": "Azithromycin Dihydrate", "labeler_name": "REMEDYREPACK INC.", "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_end_date": "20261130", "marketing_start_date": "20220829"}