Package 68071-2297-2

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 68071-2297-2
Digits Only 6807122972
Product NDC 68071-2297
Description

2 TABLET, FILM COATED in 1 BOTTLE (68071-2297-2)

Marketing

Marketing Status
Marketed Since 2020-11-16
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": "1d784ba4-83f4-0a32-e063-6294a90a63a9", "openfda": {"upc": ["0368071229721"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["b43d23c7-1a2e-ce93-e053-2995a90a65a4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-2297-2)", "package_ndc": "68071-2297-2", "marketing_start_date": "20201116"}], "brand_name": "Azithromycin", "product_id": "68071-2297_1d784ba4-83f4-0a32-e063-6294a90a63a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-2297", "generic_name": "Azithromycin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA210001", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}