ciprofloxacin

Generic: ciprofloxacin

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler northwind health company, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-490
Product ID 51655-490_490f7c8c-c3f7-bc3e-e063-6294a90af23e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208921
Listing Expiration 2027-12-31
Marketing Start 2023-01-05

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 51655490
Hyphenated Format 51655-490

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 (source: ndc)
Generic Name ciprofloxacin (source: ndc)
Application Number ANDA208921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-20)
  • 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-52)
  • 10 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-53)
  • 14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-84)
  • 6 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-87)
source: ndc

Packages (5)

51655-490-20 20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-20) 51655-490-52 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-52) 51655-490-53 10 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-53) 51655-490-84 14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-84) 51655-490-87 6 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-87)

Ingredients (1)

ciprofloxacin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "490f7c8c-c3f7-bc3e-e063-6294a90af23e", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["f6debb60-d885-230b-e053-6394a90ad73a"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-20)", "package_ndc": "51655-490-20", "marketing_start_date": "20230203"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-52)", "package_ndc": "51655-490-52", "marketing_start_date": "20230105"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-53)", "package_ndc": "51655-490-53", "marketing_start_date": "20230203"}, {"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-84)", "package_ndc": "51655-490-84", "marketing_start_date": "20230120"}, {"sample": false, "description": "6 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-87)", "package_ndc": "51655-490-87", "marketing_start_date": "20230105"}], "brand_name": "Ciprofloxacin", "product_id": "51655-490_490f7c8c-c3f7-bc3e-e063-6294a90af23e", "dosage_form": "TABLET, COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "51655-490", "generic_name": "Ciprofloxacin", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20271231"}