NDC 73377-177-01 - Ciprofloxacin

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 73377-177
Requested NDC: 73377-177-01
Package NDCs from labels: 73377-177-01
Manufacturer: AX Pharmaceutical Corp
Effective date: 2026-01-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ciprofloxacin - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2026-01-19	BULK INGREDIENT - ANIMAL DRUG

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73377-177	CIPROFLOXACIN POWDER [AX PHARMACEUTICAL CORP]	2	Unmatched	20220903_a387750b-d776-4e41-8785-1806d869cea4.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ciprofloxacin	CIPROFLOXACIN	Sagent Pharmaceuticals	f406e796-17d9-4465-b8a7-00d966a4ba74	2026-08-04	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 5E8K9I0O4U
Ciprofloxacin in Dextrose	CIPROFLOXACIN	ProPharma Distribution	42c758be-4d44-018a-e063-6294a90ae041	2025-11-04	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 5E8K9I0O4U
Ciprofloxacin in Dextrose	CIPROFLOXACIN	Hospira, Inc.	cbbbf939-3219-4515-a48e-ca264daa4d07	2025-11-04	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 5E8K9I0O4U
Ciprofloxacin	CIPROFLOXACIN	Sagent Pharmaceuticals	7049f870-6741-4a67-8033-398c36126a06	2022-09-19	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 5E8K9I0O4U

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.