Package 71610-081-83

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 71610-081-83
Digits Only 7161008183
Product NDC 71610-081
Product ID 71610-081_56c4b5b6-b49e-4bcf-a25d-ec55fbac531d
Description

3600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-081-83)

Marketing

Marketing Status
Marketed Since 2018-05-31
Brand ciprofloxacin
Generic ciprofloxacin
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": "56c4b5b6-b49e-4bcf-a25d-ec55fbac531d", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c7bc0d20-526c-48ea-b23a-cea9eb7080ff"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "3600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-081-83)", "package_ndc": "71610-081-83", "marketing_start_date": "20180531"}], "brand_name": "Ciprofloxacin", "product_id": "71610-081_56c4b5b6-b49e-4bcf-a25d-ec55fbac531d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71610-081", "generic_name": "Ciprofloxacin", "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"}