Package 67296-1848-1

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 67296-1848-1
Digits Only 6729618481
Product NDC 67296-1848
Product ID 67296-1848_2c62ea96-679a-d05f-e063-6394a90aa2d8
Description

10 TABLET, COATED in 1 BOTTLE (67296-1848-1)

Marketing

Marketing Status
Marketed Since 2020-08-12
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c62ea96-679a-d05f-e063-6394a90aa2d8", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["17435f05-f04d-e792-e063-6294a90af145"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (67296-1848-1)", "package_ndc": "67296-1848-1", "marketing_start_date": "20200812"}], "brand_name": "Ciprofloxacin", "product_id": "67296-1848_2c62ea96-679a-d05f-e063-6394a90aa2d8", "dosage_form": "TABLET, COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67296-1848", "generic_name": "Ciprofloxacin", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20261231"}