ciprofloxacin

Generic: ciprofloxacin

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler st. mary's medical park pharmacy
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
St. Mary's Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-676
Product ID 60760-676_c32cef90-e57e-2a0e-e053-2a95a90ae037
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208921
Listing Expiration 2026-12-31
Marketing Start 2021-05-21

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760676
Hyphenated Format 60760-676

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
  • 10 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-10)
  • 20 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-20)
source: ndc

Packages (2)

60760-676-10 10 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-10) 60760-676-20 20 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-20)

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": "c32cef90-e57e-2a0e-e053-2a95a90ae037", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c32ccb5f-b9d7-0aff-e053-2995a90afe6d"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-10)", "package_ndc": "60760-676-10", "marketing_start_date": "20210528"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-20)", "package_ndc": "60760-676-20", "marketing_start_date": "20210521"}], "brand_name": "Ciprofloxacin", "product_id": "60760-676_c32cef90-e57e-2a0e-e053-2a95a90ae037", "dosage_form": "TABLET, COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "60760-676", "generic_name": "Ciprofloxacin", "labeler_name": "St. Mary's Medical Park Pharmacy", "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": "20210521", "listing_expiration_date": "20261231"}