ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin hydrochloride
Generic Name ciprofloxacin hydrochloride
Labeler proficient rx lp
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

ciprofloxacin hydrochloride 3 mg/mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-985
Product ID 63187-985_6d644d3b-aaa3-489f-b2e7-5a9a5e2ac903
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA019992
Listing Expiration 2026-12-31
Marketing Start 2004-05-07

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187985
Hyphenated Format 63187-985

Supplemental Identifiers

RxCUI
309307
UPC
0363187985059
UNII
4BA73M5E37

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ciprofloxacin hydrochloride (source: ndc)
Generic Name ciprofloxacin hydrochloride (source: ndc)
Application Number NDA019992 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 3 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (63187-985-05) / 5 mL in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (63187-985-10) / 10 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

63187-985-05 1 BOTTLE, PLASTIC in 1 CARTON (63187-985-05) / 5 mL in 1 BOTTLE, PLASTIC 63187-985-10 1 BOTTLE, PLASTIC in 1 CARTON (63187-985-10) / 10 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

ciprofloxacin hydrochloride (3 mg/mL)

Linked Drug Pages (1)

Ciprofloxacin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "6d644d3b-aaa3-489f-b2e7-5a9a5e2ac903", "openfda": {"upc": ["0363187985059"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["e04dfddd-6177-4c2e-8f42-acd65848e6e2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63187-985-05)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "63187-985-05", "marketing_start_date": "20180301"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63187-985-10)  / 10 mL in 1 BOTTLE, PLASTIC", "package_ndc": "63187-985-10", "marketing_start_date": "20181201"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "63187-985_6d644d3b-aaa3-489f-b2e7-5a9a5e2ac903", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "63187-985", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "NDA019992", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20040507", "listing_expiration_date": "20261231"}