Package 71205-997-30

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-997-30
Digits Only 7120599730
Product NDC 71205-997
Product ID 71205-997_1c1b4148-3301-4ab7-8955-667658b4c133
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30)

Marketing

Marketing Status
Marketed Since 2020-03-25
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": "1c1b4148-3301-4ab7-8955-667658b4c133", "openfda": {"upc": ["0371205997304"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a093ca6e-9963-4eea-b60d-6e2f148192ec"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71205-997-00)", "package_ndc": "71205-997-00", "marketing_start_date": "20200325"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-997-10)", "package_ndc": "71205-997-10", "marketing_start_date": "20200325"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71205-997-14)", "package_ndc": "71205-997-14", "marketing_start_date": "20200325"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-997-20)", "package_ndc": "71205-997-20", "marketing_start_date": "20200325"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30)", "package_ndc": "71205-997-30", "marketing_start_date": "20200325"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55)", "package_ndc": "71205-997-55", "marketing_start_date": "20200325"}], "brand_name": "Ciprofloxacin", "product_id": "71205-997_1c1b4148-3301-4ab7-8955-667658b4c133", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-997", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}