Package 68788-8800-6

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 68788-8800-6
Digits Only 6878888006
Product NDC 68788-8800
Description

1 BLISTER PACK in 1 CARTON (68788-8800-6) / 6 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-01-01
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": "743a81de-0dea-4b20-b00c-76b89ec62797", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["b3c84aea-7ba7-4aae-999c-db740a9e53df"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68788-8800-6)  / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68788-8800-6", "marketing_start_date": "20250101"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68788-8800_743a81de-0dea-4b20-b00c-76b89ec62797", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68788-8800", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Preferred 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": "20250101", "listing_expiration_date": "20271231"}