Package 0904-7351-04

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 0904-7351-04
Digits Only 0904735104
Product NDC 0904-7351
Product ID 0904-7351_7cae275e-abb8-4fad-af20-fa3fdbf095e5
Description

30 BLISTER PACK in 1 CARTON (0904-7351-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-05-01
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": "7cae275e-abb8-4fad-af20-fa3fdbf095e5", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "308460"], "spl_set_id": ["814abe38-da4a-48af-bf4b-2ce04a5aabd1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7351-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7351-04", "marketing_start_date": "20230501"}], "brand_name": "azithromycin", "product_id": "0904-7351_7cae275e-abb8-4fad-af20-fa3fdbf095e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0904-7351", "generic_name": "azithromycin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA065399", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}