ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin hydrochloride
Generic Name ciprofloxacin hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7843
Product ID 50090-7843_56da4ad6-dcd2-4df7-b174-e78c8e0127b6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076593
Listing Expiration 2027-12-31
Marketing Start 2024-05-23

Pharmacologic Class

Classes
cytochrome p450 1a2 inhibitors [moa] fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907843
Hyphenated Format 50090-7843

Supplemental Identifiers

RxCUI
309309
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 ANDA076593 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-7843-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (50090-7843-1)
  • 6 TABLET, FILM COATED in 1 BOTTLE (50090-7843-3)
  • 28 TABLET, FILM COATED in 1 BOTTLE (50090-7843-4)
  • 10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7843-7)
  • 1 TABLET, FILM COATED in 1 BOTTLE (50090-7843-8)
source: ndc

Packages (7)

50090-7843-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-7843-0) 50090-7843-1 14 TABLET, FILM COATED in 1 BOTTLE (50090-7843-1) 50090-7843-3 6 TABLET, FILM COATED in 1 BOTTLE (50090-7843-3) 50090-7843-4 28 TABLET, FILM COATED in 1 BOTTLE (50090-7843-4) 50090-7843-5 10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5) 50090-7843-7 30 TABLET, FILM COATED in 1 BOTTLE (50090-7843-7) 50090-7843-8 1 TABLET, FILM COATED in 1 BOTTLE (50090-7843-8)

Ingredients (1)

ciprofloxacin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Ciprofloxacin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56da4ad6-dcd2-4df7-b174-e78c8e0127b6", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["6d029ad2-a1e8-4c11-a5eb-e2257c6a0ddb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-7843-0)", "package_ndc": "50090-7843-0", "marketing_start_date": "20251230"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-7843-1)", "package_ndc": "50090-7843-1", "marketing_start_date": "20251230"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-7843-3)", "package_ndc": "50090-7843-3", "marketing_start_date": "20251230"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (50090-7843-4)", "package_ndc": "50090-7843-4", "marketing_start_date": "20251230"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5)", "package_ndc": "50090-7843-5", "marketing_start_date": "20251230"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7843-7)", "package_ndc": "50090-7843-7", "marketing_start_date": "20251230"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE (50090-7843-8)", "package_ndc": "50090-7843-8", "marketing_start_date": "20251230"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "50090-7843_56da4ad6-dcd2-4df7-b174-e78c8e0127b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7843", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076593", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20271231"}