Package 68071-3715-4

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 68071-3715-4
Digits Only 6807137154
Product NDC 68071-3715
Product ID 68071-3715_2a32433c-0956-9672-e063-6394a90a1ac3
Description

4 TABLET, FILM COATED in 1 BOTTLE (68071-3715-4)

Marketing

Marketing Status
Marketed Since 2024-10-28
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a32433c-0956-9672-e063-6394a90a1ac3", "openfda": {"upc": ["0368071371543"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["258dd3c5-dce9-7483-e063-6294a90a4043"], "manufacturer_name": ["NuCare Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-3715-4)", "package_ndc": "68071-3715-4", "marketing_start_date": "20241028"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68071-3715_2a32433c-0956-9672-e063-6394a90a1ac3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-3715", "generic_name": "Azithromycin Dihydrate", "labeler_name": "NuCare Pharmaceuticals 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_start_date": "20240215", "listing_expiration_date": "20261231"}