Package 71205-300-05

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 71205-300-05
Digits Only 7120530005
Product NDC 71205-300
Product ID 71205-300_a797de06-c8be-4417-9bac-137dc4931c8b
Description

1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05) / 5 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2018-11-01
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "a797de06-c8be-4417-9bac-137dc4931c8b", "openfda": {"upc": ["0371205300050"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["05b2836d-cd3d-4d7f-970c-66ec2d788667"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "71205-300-05", "marketing_start_date": "20181101"}], "brand_name": "ciprofloxacin", "product_id": "71205-300_a797de06-c8be-4417-9bac-137dc4931c8b", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-300", "generic_name": "Ciprofloxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "ANDA077568", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}