ciprofloxacin

Generic: ciprofloxacin hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-330
Product ID 72789-330_3cf6f764-1e6f-6036-e063-6294a90aa8e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Marketing Start 2007-04-26
Marketing End 2027-02-28

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 72789330
Hyphenated Format 72789-330

Supplemental Identifiers

RxCUI
309309
UPC
0372789330204
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
  • 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-06)
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-20)
  • 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-28)
source: ndc

Packages (5)

72789-330-06 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-06) 72789-330-10 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-10) 72789-330-14 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-14) 72789-330-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-20) 72789-330-28 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-28)

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": "3cf6f764-1e6f-6036-e063-6294a90aa8e9", "openfda": {"upc": ["0372789330204"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a2ffa81a-86c5-40b9-8fa0-c889801ef479"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-06)", "package_ndc": "72789-330-06", "marketing_end_date": "20270228", "marketing_start_date": "20230830"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-10)", "package_ndc": "72789-330-10", "marketing_end_date": "20270228", "marketing_start_date": "20230907"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-14)", "package_ndc": "72789-330-14", "marketing_end_date": "20270228", "marketing_start_date": "20230814"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-20)", "package_ndc": "72789-330-20", "marketing_end_date": "20270228", "marketing_start_date": "20230706"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-28)", "package_ndc": "72789-330-28", "marketing_end_date": "20270228", "marketing_start_date": "20230807"}], "brand_name": "Ciprofloxacin", "product_id": "72789-330_3cf6f764-1e6f-6036-e063-6294a90aa8e9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-330", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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_end_date": "20270228", "marketing_start_date": "20070426"}