Package 68999-309-20

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68999-309-20
Digits Only 6899930920
Product NDC 68999-309
Product ID 68999-309_f049eb75-5f01-5caa-e053-2a95a90a804c
Description

20 TABLET, FILM COATED in 1 BOTTLE (68999-309-20)

Marketing

Marketing Status
Marketed Since 2020-05-26
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": "f049eb75-5f01-5caa-e053-2a95a90a804c", "openfda": {"upc": ["0368999309284"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["d40f0560-fc57-4f00-9f6d-ae7e2a274330"], "manufacturer_name": ["CHARTWELL GOVERNMENTAL & SPECIALTY RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68999-309-20)", "package_ndc": "68999-309-20", "marketing_start_date": "20200526"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68999-309-28)", "package_ndc": "68999-309-28", "marketing_start_date": "20200526"}], "brand_name": "Ciprofloxacin", "product_id": "68999-309_f049eb75-5f01-5caa-e053-2a95a90a804c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68999-309", "generic_name": "Ciprofloxacin hydrochloride", "labeler_name": "CHARTWELL GOVERNMENTAL & SPECIALTY RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}