Package 50090-7848-1
Brand: ciprofloxacin hydrochloride
Generic: ciprofloxacin hydrochloridePackage Facts
Identity
Package NDC
50090-7848-1
Digits Only
5009078481
Product NDC
50090-7848
Description
14 TABLET, FILM COATED in 1 BOTTLE (50090-7848-1)
Marketing
Marketing Status
Brand
ciprofloxacin hydrochloride
Generic
ciprofloxacin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0865c2c3-d66b-407c-a9bc-8a25c9f2b20d", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["1057be77-00bb-4839-be3d-c8e11ae531a2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-7848-1)", "package_ndc": "50090-7848-1", "marketing_start_date": "20260105"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "50090-7848_0865c2c3-d66b-407c-a9bc-8a25c9f2b20d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7848", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076593", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20271231"}