Package 50090-3852-0

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3852-0
Digits Only 5009038520
Product NDC 50090-3852
Product ID 50090-3852_ee3193b9-9650-4cd6-bb66-b1e43c8461ed
Description

20 TABLET, FILM COATED in 1 BOTTLE (50090-3852-0)

Marketing

Marketing Status
Marketed Since 2018-11-20
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
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": "ee3193b9-9650-4cd6-bb66-b1e43c8461ed", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["d8b21832-b74f-4f85-a304-b907c9e01e72"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-3852-0)", "package_ndc": "50090-3852-0", "marketing_start_date": "20181120"}], "brand_name": "Ciprofloxacin", "product_id": "50090-3852_ee3193b9-9650-4cd6-bb66-b1e43c8461ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-3852", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}