ciprofloxacin

Generic: ciprofloxacin

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler rising pharma holdings, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 750 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-413
Product ID 16571-413_f031ce92-a4ed-45b0-8eb3-c3bdb02fbece
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076639
Listing Expiration 2026-12-31
Marketing Start 2004-09-10

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 16571413
Hyphenated Format 16571-413

Supplemental Identifiers

RxCUI
197511 197512 309309
UPC
0316577411102 0316571412501
UNII
4BA73M5E37

Packaging Origin

Original Packager
true

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 ANDA076639 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED in 1 BOTTLE (16571-413-05)
source: ndc

Packages (1)

16571-413-05 50 TABLET, FILM COATED in 1 BOTTLE (16571-413-05)

Ingredients (1)

ciprofloxacin hydrochloride (750 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": "f031ce92-a4ed-45b0-8eb3-c3bdb02fbece", "openfda": {"upc": ["0316577411102", "0316571412501"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["ef468722-68cd-440b-afd7-2285029db41f"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (16571-413-05)", "package_ndc": "16571-413-05", "marketing_start_date": "20040910"}], "brand_name": "ciprofloxacin", "product_id": "16571-413_f031ce92-a4ed-45b0-8eb3-c3bdb02fbece", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "16571-413", "generic_name": "ciprofloxacin", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}