Package 68094-690-30

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 68094-690-30
Digits Only 6809469030
Product NDC 68094-690
Description

30 TABLET, FILM COATED in 1 BOTTLE (68094-690-30)

Marketing

Marketing Status
Marketed Since 2024-02-15
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": "5d373887-5ca3-4911-bd76-0ff51141df5f", "openfda": {"upc": ["0368094690300"], "unii": ["5FD1131I7S"], "rxcui": ["204844"], "spl_set_id": ["b88f5839-8e8b-4bf6-a577-5c8b7cffeec6"], "manufacturer_name": ["Precision Dose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68094-690-30)", "package_ndc": "68094-690-30", "marketing_start_date": "20240215"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68094-690_5d373887-5ca3-4911-bd76-0ff51141df5f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68094-690", "generic_name": "Azithromycin dihydrate", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA207566", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}