Package 60429-042-20
Brand: ciprofloxacin
Generic: ciprofloxacinPackage Facts
Identity
Package NDC
60429-042-20
Digits Only
6042904220
Product NDC
60429-042
Description
20 TABLET, FILM COATED in 1 BOTTLE (60429-042-20)
Marketing
Marketing Status
Brand
ciprofloxacin
Generic
ciprofloxacin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bc37c4b-f0da-5e5f-e063-6294a90a0760", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["2e1addcf-6d5b-46c8-812b-558fd847f005"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (60429-042-20)", "package_ndc": "60429-042-20", "marketing_start_date": "20141103"}], "brand_name": "Ciprofloxacin", "product_id": "60429-042_2bc37c4b-f0da-5e5f-e063-6294a90a0760", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "60429-042", "generic_name": "Ciprofloxacin", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20040609", "listing_expiration_date": "20261231"}