Package 71205-636-06

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-636-06
Digits Only 7120563606
Product NDC 71205-636
Description

6 TABLET, FILM COATED in 1 BOTTLE (71205-636-06)

Marketing

Marketing Status
Marketed Since 2022-02-02
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e72981fd-0d15-473b-8e3d-ee84e3d71c03", "openfda": {"upc": ["0371205636104"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["9ee1f252-a64e-4b72-a6f7-60298e827222"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71205-636-06)", "package_ndc": "71205-636-06", "marketing_start_date": "20220202"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-636-10)", "package_ndc": "71205-636-10", "marketing_start_date": "20220202"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71205-636-14)", "package_ndc": "71205-636-14", "marketing_start_date": "20220203"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-636-20)", "package_ndc": "71205-636-20", "marketing_start_date": "20220202"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-636-30)", "package_ndc": "71205-636-30", "marketing_start_date": "20220202"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-636-60)", "package_ndc": "71205-636-60", "marketing_start_date": "20220202"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-636-90)", "package_ndc": "71205-636-90", "marketing_start_date": "20220202"}], "brand_name": "Ciprofloxacin", "product_id": "71205-636_e72981fd-0d15-473b-8e3d-ee84e3d71c03", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-636", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}