ciprofloxacin

Generic: ciprofloxacin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 3 mg/mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-300
Product ID 71205-300_a797de06-c8be-4417-9bac-137dc4931c8b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077568
Listing Expiration 2026-12-31
Marketing Start 2018-11-01

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205300
Hyphenated Format 71205-300

Supplemental Identifiers

RxCUI
309307
UPC
0371205300050
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 (source: ndc)
Generic Name ciprofloxacin (source: ndc)
Application Number ANDA077568 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 3 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05) / 5 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

71205-300-05 1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05) / 5 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

ciprofloxacin hydrochloride (3 mg/mL)

Linked Drug Pages (1)

ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "a797de06-c8be-4417-9bac-137dc4931c8b", "openfda": {"upc": ["0371205300050"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["05b2836d-cd3d-4d7f-970c-66ec2d788667"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "71205-300-05", "marketing_start_date": "20181101"}], "brand_name": "ciprofloxacin", "product_id": "71205-300_a797de06-c8be-4417-9bac-137dc4931c8b", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-300", "generic_name": "Ciprofloxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "ANDA077568", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}