Package 69306-250-06

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 69306-250-06
Digits Only 6930625006
Product NDC 69306-250
Product ID 69306-250_c479da04-f3f7-fa5f-e053-2995a90a9ef8
Description

6 TABLET, FILM COATED in 1 BLISTER PACK (69306-250-06)

Marketing

Marketing Status
Marketed Since 2020-04-11
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (1)

Azithromycin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c479da04-f3f7-fa5f-e053-2995a90a9ef8", "openfda": {"upc": ["0369306250060"], "unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["90ff7cfc-73c9-4d77-83df-c05cfbbbbecd"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BLISTER PACK (69306-250-06)", "package_ndc": "69306-250-06", "marketing_start_date": "20200411"}], "brand_name": "Azithromycin", "product_id": "69306-250_c479da04-f3f7-fa5f-e053-2995a90a9ef8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "69306-250", "generic_name": "Azithromycin", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA210000", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}