Package 68071-3693-6

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 68071-3693-6
Digits Only 6807136936
Product NDC 68071-3693
Product ID 68071-3693_238284a8-b38f-82af-e063-6394a90a79e1
Description

6 TABLET in 1 BOTTLE (68071-3693-6)

Marketing

Marketing Status
Marketed Since 2024-10-02
Brand ciprofloxacin
Generic ciprofolxacin
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": "238284a8-b38f-82af-e063-6394a90a79e1", "openfda": {"upc": ["0368071369366"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["238284a8-b38e-82af-e063-6394a90a79e1"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-3693-6)", "package_ndc": "68071-3693-6", "marketing_start_date": "20241002"}], "brand_name": "Ciprofloxacin", "product_id": "68071-3693_238284a8-b38f-82af-e063-6394a90a79e1", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-3693", "generic_name": "Ciprofolxacin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}