NDC 59115-030-55 - 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: 59115-030
Requested NDC: 59115-030-55
Package NDCs from labels: 59115-030-25, 59115-030-01, 59115-030-33, 59115-030-55
Manufacturer: Hikma Pharmaceutical
Effective date: 2014-08-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ciprofloxacin - Hikma Pharmaceutical	Hikma Pharmaceutical	2014-08-20	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CIPROFLOXACIN HYDROCHLORIDE	ACTIVE INGREDIENT	4BA73M5E37	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
CIPROFLOXACIN	ACTIVE MOIETY	5E8K9I0O4U	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4
WATER	INACTIVE INGREDIENT	059QF0KO0R	CIPROFLOXACIN TABLET, FILM COATED [HIKMA PHARMACEUTICAL]	4

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 147 of 147 · 2,926 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meijer Baby Tear Free SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	Meijer Distributing Inc.	2434de23-bcc9-4a83-9945-16fc3f2b8c61	2016-06-01	Warnings	Exact identifier unii: 15FIX9V2JP
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted)	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	6a996e03-907f-4e6a-b232-0892b86956b0	2015-08-21	Warnings	Exact identifier unii: 15FIX9V2JP
Renewal Firming Day Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	BURT'S BEES, INC.	18ceb5d8-4b76-6a54-e054-00144ff88e88	2015-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
5268c4b9-0e68-4aa2-a75b-5ed1e77c4318			aebc9dc3-d1a5-4fb5-97c6-3bcd87a44fac	2014-08-20	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: 5268c4b9-0e68-4aa2-a75b-5ed1e77c4318 spl set id: aebc9dc3-d1a5-4fb5-97c6-3bcd87a44fac
TiZO2	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD.	30468afc-9616-4765-b046-12e97a0a7827	2010-12-20	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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