Package 82804-153-04

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 82804-153-04
Digits Only 8280415304
Product NDC 82804-153
Product ID 82804-153_edecf20d-c681-418b-9c47-02fb32d2b3c0
Description

4 TABLET, FILM COATED in 1 BOTTLE (82804-153-04)

Marketing

Marketing Status
Marketed Since 2024-09-25
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "edecf20d-c681-418b-9c47-02fb32d2b3c0", "openfda": {"upc": ["0382804153046"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["edecf20d-c681-418b-9c47-02fb32d2b3c0"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (82804-153-04)", "package_ndc": "82804-153-04", "marketing_start_date": "20240925"}], "brand_name": "Azithromycin Dihydrate", "product_id": "82804-153_edecf20d-c681-418b-9c47-02fb32d2b3c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "82804-153", "generic_name": "Azithromycin dihydrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}