Package 68788-7598-3

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 68788-7598-3
Digits Only 6878875983
Product NDC 68788-7598
Description

3 TABLET, FILM COATED in 1 BLISTER PACK (68788-7598-3)

Marketing

Marketing Status
Marketed Since 2020-02-13
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": "037b0da7-6b6b-4cce-bb28-05597873a467", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["003307c5-3f73-4a5d-a704-bfdea3c656e8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BLISTER PACK (68788-7598-3)", "package_ndc": "68788-7598-3", "marketing_start_date": "20200213"}], "brand_name": "Azithromycin", "product_id": "68788-7598_037b0da7-6b6b-4cce-bb28-05597873a467", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68788-7598", "generic_name": "Azithromycin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA207398", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20261231"}