Package 62135-310-28

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-310-28
Digits Only 6213531028
Product NDC 62135-310
Product ID 62135-310_410cec1e-83d0-dbed-e063-6394a90a6513
Description

28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-310-28)

Marketing

Marketing Status
Marketed Since 2021-04-13
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": "410cec1e-83d0-dbed-e063-6394a90a6513", "openfda": {"upc": ["0362135309206", "0362135309107", "0362135309053", "0362135309015", "0362135310202", "0362135309282", "0362135308018", "0362135308209", "0362135310288", "0362135308285", "0362135310509"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["6c64aa79-d087-4568-904c-3a0638b91e69"], "manufacturer_name": ["Chartwell RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-310-20)", "package_ndc": "62135-310-20", "marketing_start_date": "20210413"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-310-28)", "package_ndc": "62135-310-28", "marketing_start_date": "20210413"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-310-50)", "package_ndc": "62135-310-50", "marketing_start_date": "20210413"}], "brand_name": "Ciprofloxacin", "product_id": "62135-310_410cec1e-83d0-dbed-e063-6394a90a6513", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "62135-310", "generic_name": "Ciprofloxacin hydrochloride", "labeler_name": "Chartwell RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076896", "marketing_category": "ANDA", "marketing_start_date": "20210413", "listing_expiration_date": "20261231"}