Package 72189-323-06

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 72189-323-06
Digits Only 7218932306
Product NDC 72189-323
Product ID 72189-323_2c3d4146-03d9-30a9-e063-6294a90ad471
Description

6 TABLET, COATED in 1 BOTTLE (72189-323-06)

Marketing

Marketing Status
Marketed Since 2022-02-21
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": ["ORAL"], "spl_id": "2c3d4146-03d9-30a9-e063-6294a90ad471", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["d88a22f4-2f61-17f2-e053-2995a90acd14"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, COATED in 1 BOTTLE (72189-323-06)", "package_ndc": "72189-323-06", "marketing_start_date": "20220221"}], "brand_name": "CIPROFLOXACIN", "product_id": "72189-323_2c3d4146-03d9-30a9-e063-6294a90ad471", "dosage_form": "TABLET, COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-323", "generic_name": "CIPROFLOXACIN", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPROFLOXACIN", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20220221", "listing_expiration_date": "20261231"}