Package 43063-923-30

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-923-30
Digits Only 4306392330
Product NDC 43063-923
Product ID 43063-923_42ef92d0-be54-bc1c-e063-6294a90aa576
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-923-30)

Marketing

Marketing Status
Marketed Since 2019-05-10
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": "42ef92d0-be54-bc1c-e063-6294a90aa576", "openfda": {"upc": ["0343063923207"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["cfda82e4-8660-447e-a881-b87165a31e9a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-923-30)", "package_ndc": "43063-923-30", "marketing_start_date": "20190510"}], "brand_name": "Ciprofloxacin", "product_id": "43063-923_42ef92d0-be54-bc1c-e063-6294a90aa576", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "43063-923", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}