Ciprofloxacin

Product NDC
64205-927
11-digit product format
642050927
Labeler code
64205
Product ID
64205-927_74bf41a6-b284-42fd-a08a-4fc8d7213c7d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ReadyMeds
Application
ANDA076558
Marketing category
ANDA
Marketing start
2004-06-09
Marketing end
0000-00-00
Substance
CIPROFLOXACIN HYDROCHLORIDE
Active strength
250 mg/1
Pharmacologic classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ea50b939-d92a-4100-84f5-1c1089663837Product name220240705
90aab9f8-63f3-478d-8db8-951525a18ab1Product name120180814
200e1d3d-46da-4371-beed-747da3cb3ff8Product name120180702
9e453f34-aacb-44d5-a119-c0e3dc1fca2aProduct name120160622
01eecbfe-0b50-413b-8898-6905c89b6568Product name120151228
a3304bb6-ef4e-06df-d604-35f7e883ed6cProduct name120140508
abaf203f-619e-f265-559f-8c81af5cb1c2Product name120140508
de5ea793-ffd9-0308-b0ca-00d9967be4eeProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64205-927-142019-11-27C16284748780-19855e2a2-3f0c-60a7-e053-dbdaa90a05bdCiprofloxacin Tablets, USP Rev. 09/13 Rx Only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64205-927-14Ciprofloxacin14 in 1 BOTTLETABLET, FILM COATED148

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CIPROFLOXACIN HYDROCHLORIDEACTIVE INGREDIENT4BA73M5E37CIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
CIPROFLOXACINACTIVE MOIETY5E8K9I0O4UCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ACIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4CIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2CIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
TALCINACTIVE INGREDIENT7SEV7J4R1UCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8
WATERINACTIVE INGREDIENT059QF0KO0RCIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64205-927CIPROFLOXACIN TABLET, FILM COATED [READYMEDS]8Legacy NDC, 1 package rows20140515_8916b85c-9004-4e26-a34d-b0e6a65e6a24.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197511ciprofloxacin 250 MG Oral TabletPSN8916b85c-9004-4e26-a34d-b0e6a65e6a248
309309ciprofloxacin 500 MG Oral TabletPSN8916b85c-9004-4e26-a34d-b0e6a65e6a248
197511ciprofloxacin 250 MG Oral TabletSCD8916b85c-9004-4e26-a34d-b0e6a65e6a248
309309ciprofloxacin 500 MG Oral TabletSCD8916b85c-9004-4e26-a34d-b0e6a65e6a248
309309ciprofloxacin (as ciprofloxacin HCl) 500 MG Oral TabletSY8916b85c-9004-4e26-a34d-b0e6a65e6a248
197511ciprofloxacin 250 MG (as ciprofloxacin HCl 297 MG) Oral TabletSY8916b85c-9004-4e26-a34d-b0e6a65e6a248

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
64205-927-146420509271414 in 1 BOTTLEHistorical