Package 68788-8702-6

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 68788-8702-6
Digits Only 6878887026
Product NDC 68788-8702
Description

1 BLISTER PACK in 1 CARTON (68788-8702-6) / 6 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-06-27
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": "467c8932-77a6-42e9-a9a6-a57f9a021904", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["4eec460d-5ba8-4614-8700-219a9b4fc385"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68788-8702-6)  / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68788-8702-6", "marketing_start_date": "20240627"}], "brand_name": "Azithromycin", "product_id": "68788-8702_467c8932-77a6-42e9-a9a6-a57f9a021904", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68788-8702", "generic_name": "Azithromycin", "labeler_name": "Preferred Pharmaceuticals 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": "20240627", "listing_expiration_date": "20261231"}