ofloxacin
Generic: ofloxacin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ofloxacin
Generic Name
ofloxacin
Labeler
a-s medication solutions
Dosage Form
SOLUTION
Routes
Active Ingredients
ofloxacin 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5209
Product ID
50090-5209_14be937e-e144-4507-aef1-cf5b3c8e2d6b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076513
Listing Expiration
2026-12-31
Marketing Start
2019-03-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905209
Hyphenated Format
50090-5209
Supplemental Identifiers
RxCUI
UNII
NUI
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
ofloxacin (source: ndc)
Generic Name
ofloxacin (source: ndc)
Application Number
ANDA076513 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (50090-5209-0) / 5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "14be937e-e144-4507-aef1-cf5b3c8e2d6b", "openfda": {"nui": ["N0000175937", "M0023650"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["ab5b0e34-ac5c-4c0c-b104-934b319ae011"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (50090-5209-0) / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "50090-5209-0", "marketing_start_date": "20201005"}], "brand_name": "Ofloxacin", "product_id": "50090-5209_14be937e-e144-4507-aef1-cf5b3c8e2d6b", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "50090-5209", "generic_name": "ofloxacin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ofloxacin", "active_ingredients": [{"name": "OFLOXACIN", "strength": "3 mg/mL"}], "application_number": "ANDA076513", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}