Package 71205-420-05

Brand: ofloxacin

Generic: ofloxacin
NDC Package

Package Facts

Identity

Package NDC 71205-420-05
Digits Only 7120542005
Product NDC 71205-420
Description

1 BOTTLE, DROPPER in 1 CARTON (71205-420-05) / 5 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2020-03-01
Brand ofloxacin
Generic ofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "e65f9309-c5da-4159-ba09-28754fe12593", "openfda": {"nui": ["N0000175937", "M0023650"], "upc": ["0371205420055"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["5a9de529-6f85-467a-97b0-8ce124c31173"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (71205-420-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "71205-420-05", "marketing_start_date": "20200301"}], "brand_name": "Ofloxacin", "product_id": "71205-420_e65f9309-c5da-4159-ba09-28754fe12593", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-420", "generic_name": "ofloxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ofloxacin", "active_ingredients": [{"name": "OFLOXACIN", "strength": "3 mg/mL"}], "application_number": "ANDA076513", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}