Package 50419-754-01

Brand: cipro

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50419-754-01
Digits Only 5041975401
Product NDC 50419-754
Product ID 50419-754_1b112839-6cf0-466a-9188-86fc5b1549f9
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01)

Marketing

Marketing Status
Marketed Since 1987-10-22
Brand cipro
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Cipro ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b112839-6cf0-466a-9188-86fc5b1549f9", "openfda": {"upc": ["0350419754019", "0350419758017"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "205769", "205770", "213224", "213226", "309308", "309309", "309310"], "spl_set_id": ["888dc7f9-ad9c-4c00-8d50-8ddfd9bd27c0"], "manufacturer_name": ["Bayer HealthCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01)", "package_ndc": "50419-754-01", "marketing_start_date": "19871022"}], "brand_name": "Cipro", "product_id": "50419-754_1b112839-6cf0-466a-9188-86fc5b1549f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50419-754", "generic_name": "ciprofloxacin hydrochloride", "labeler_name": "Bayer HealthCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cipro", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "NDA019537", "marketing_category": "NDA", "marketing_start_date": "19871022", "listing_expiration_date": "20271231"}