Package 0781-8091-31

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 0781-8091-31
Digits Only 0781809131
Product NDC 0781-8091
Product ID 0781-8091_5cec3961-a2a4-4f61-a73e-1656021b4195
Description

30 TABLET, FILM COATED in 1 BOTTLE (0781-8091-31)

Marketing

Marketing Status
Marketed Since 2019-02-14
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": "5cec3961-a2a4-4f61-a73e-1656021b4195", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["204844"], "spl_set_id": ["34b70c23-92a6-460f-8dbb-15a0e6b9d3a9"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0781-8091-31)", "package_ndc": "0781-8091-31", "marketing_start_date": "20190214"}], "brand_name": "Azithromycin", "product_id": "0781-8091_5cec3961-a2a4-4f61-a73e-1656021b4195", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0781-8091", "generic_name": "Azithromycin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA065209", "marketing_category": "ANDA", "marketing_start_date": "20051114", "listing_expiration_date": "20261231"}