Package 71610-109-30

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-109-30
Digits Only 7161010930
Product NDC 71610-109
Product ID 71610-109_32ff40df-b3ad-4156-818b-587837737309
Description

30 TABLET, FILM COATED in 1 BOTTLE (71610-109-30)

Marketing

Marketing Status
Marketed Since 2018-09-06
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": "32ff40df-b3ad-4156-818b-587837737309", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["df24efa3-c9a0-4f40-92ce-cc71c708931b"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-109-30)", "package_ndc": "71610-109-30", "marketing_start_date": "20180906"}], "brand_name": "Ciprofloxacin", "product_id": "71610-109_32ff40df-b3ad-4156-818b-587837737309", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71610-109", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}