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 250 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-302
Product ID 72789-302_3cf6c52b-1263-b5f5-e063-6394a90a9ef7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Marketing Start 2007-04-26
Marketing End 2027-01-31

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 72789302
Hyphenated Format 72789-302

Supplemental Identifiers

RxCUI
197511
UPC
0372789302065
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
  • 250 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-06)
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-10)
  • 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-12)
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-20)
source: ndc

Packages (5)

72789-302-06 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-06) 72789-302-10 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-10) 72789-302-12 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-12) 72789-302-14 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-14) 72789-302-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-20)

Ingredients (1)

ciprofloxacin hydrochloride (250 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": "3cf6c52b-1263-b5f5-e063-6394a90a9ef7", "openfda": {"upc": ["0372789302065"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["ef07c7f4-4ccf-44f6-aee9-add6d3b0b9d2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-06)", "package_ndc": "72789-302-06", "marketing_end_date": "20270131", "marketing_start_date": "20230327"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-10)", "package_ndc": "72789-302-10", "marketing_end_date": "20270131", "marketing_start_date": "20230301"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-12)", "package_ndc": "72789-302-12", "marketing_end_date": "20270131", "marketing_start_date": "20230410"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-14)", "package_ndc": "72789-302-14", "marketing_end_date": "20270131", "marketing_start_date": "20230516"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-20)", "package_ndc": "72789-302-20", "marketing_end_date": "20270131", "marketing_start_date": "20230814"}], "brand_name": "Ciprofloxacin", "product_id": "72789-302_3cf6c52b-1263-b5f5-e063-6394a90a9ef7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-302", "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": "250 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20070426"}