ciprofloxacin

Generic: ciprofloxacin hydrochloride

Labeler: chartwell governmental & specialty rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler chartwell governmental & specialty rx llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
CHARTWELL GOVERNMENTAL & SPECIALTY RX LLC

Identifiers & Regulatory

Product NDC 68999-309
Product ID 68999-309_f049eb75-5f01-5caa-e053-2a95a90a804c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Listing Expiration 2026-12-31
Marketing Start 2007-04-26

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68999309
Hyphenated Format 68999-309

Supplemental Identifiers

RxCUI
309309
UPC
0368999309284
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 hydrochloride (source: ndc)
Application Number ANDA077859 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (68999-309-20)
  • 28 TABLET, FILM COATED in 1 BOTTLE (68999-309-28)
source: ndc

Packages (2)

68999-309-20 20 TABLET, FILM COATED in 1 BOTTLE (68999-309-20) 68999-309-28 28 TABLET, FILM COATED in 1 BOTTLE (68999-309-28)

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": "f049eb75-5f01-5caa-e053-2a95a90a804c", "openfda": {"upc": ["0368999309284"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["d40f0560-fc57-4f00-9f6d-ae7e2a274330"], "manufacturer_name": ["CHARTWELL GOVERNMENTAL & SPECIALTY RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68999-309-20)", "package_ndc": "68999-309-20", "marketing_start_date": "20200526"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68999-309-28)", "package_ndc": "68999-309-28", "marketing_start_date": "20200526"}], "brand_name": "Ciprofloxacin", "product_id": "68999-309_f049eb75-5f01-5caa-e053-2a95a90a804c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68999-309", "generic_name": "Ciprofloxacin hydrochloride", "labeler_name": "CHARTWELL GOVERNMENTAL & SPECIALTY RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}