Package 70934-965-20

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70934-965-20
Digits Only 7093496520
Product NDC 70934-965
Product ID 70934-965_e10891a7-9e65-ca14-e053-2995a90afa2f
Description

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-20)

Marketing

Marketing Status
Discontinued 2026-08-31
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": "e10891a7-9e65-ca14-e053-2995a90afa2f", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["de0b9579-fb85-e1ce-e053-2a95a90aeecb"], "manufacturer_name": ["Denton Pharma, Inc. DBA Northwind Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-06)", "package_ndc": "70934-965-06", "marketing_end_date": "20260831", "marketing_start_date": "20220502"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-14)", "package_ndc": "70934-965-14", "marketing_end_date": "20260831", "marketing_start_date": "20220502"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-20)", "package_ndc": "70934-965-20", "marketing_end_date": "20260831", "marketing_start_date": "20220502"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-30)", "package_ndc": "70934-965-30", "marketing_end_date": "20260831", "marketing_start_date": "20220516"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-60)", "package_ndc": "70934-965-60", "marketing_end_date": "20260831", "marketing_start_date": "20220609"}], "brand_name": "Ciprofloxacin", "product_id": "70934-965_e10891a7-9e65-ca14-e053-2995a90afa2f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "70934-965", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Denton Pharma, Inc. DBA Northwind Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20220502"}