Package 54348-662-06

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 54348-662-06
Digits Only 5434866206
Product NDC 54348-662
Description

1 BOTTLE in 1 BOX (54348-662-06) / 6 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-07-10
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": "ea938405-8d24-fa08-e053-2995a90af8dc", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["e2902d14-16bb-46a9-a45a-4f1f9b0ecf4a"], "manufacturer_name": ["PharmPak, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (54348-662-06)  / 6 TABLET in 1 BOTTLE", "package_ndc": "54348-662-06", "marketing_start_date": "20190710"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-662-14)  / 14 TABLET in 1 BOTTLE", "package_ndc": "54348-662-14", "marketing_start_date": "20190710"}], "brand_name": "ciprofloxacin", "product_id": "54348-662_ea938405-8d24-fa08-e053-2995a90af8dc", "dosage_form": "TABLET", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "54348-662", "generic_name": "CIPROFLOXACIN", "labeler_name": "PharmPak, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20190710", "listing_expiration_date": "20261231"}