ciprofloxacin
Generic: ciprofloxacin
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ciprofloxacin
Generic Name
ciprofloxacin
Labeler
preferred pharmaceuticals, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
ciprofloxacin hydrochloride 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7500
Product ID
68788-7500_bbc3e786-14b4-4048-8c0e-8d00a79e02f0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077568
Listing Expiration
2027-12-31
Marketing Start
2018-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887500
Hyphenated Format
68788-7500
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (68788-7500-5) / 5 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "bbc3e786-14b4-4048-8c0e-8d00a79e02f0", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["85c48ebc-d94a-4254-86df-d2c1aff09b37"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68788-7500-5) / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "68788-7500-5", "marketing_start_date": "20191130"}], "brand_name": "ciprofloxacin", "product_id": "68788-7500_bbc3e786-14b4-4048-8c0e-8d00a79e02f0", "dosage_form": "SOLUTION", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68788-7500", "generic_name": "Ciprofloxacin", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "20271231"}