Ciprofloxacin

Basic Information

Product Name

Ciprofloxacin

FDA Product Code

70934-093

Regulatory Information

NDC Product Code

70934-093

Application Number

ANDA077859

Marketing Category

C73584

Effective Date

January 1, 2023

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use CIPROFLOXACIN TABLETS safely and effectively. See full prescribing information for CIPROFLOXACIN TABLETS. CIPROFLOXACIN tablet, for oral use Initial U.S. Approval: 1987

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

CIPROFLOXACIN HYDROCHLORIDE

Quantity: 500 mg in 1 1

Code: 4BA73M5E37

Class Code: ACTIM

SILICON DIOXIDE

Code: ETJ7Z6XBU4

Class Code: IACT

MICROCRYSTALLINE CELLULOSE

Code: OP1R32D61U

Class Code: IACT

HYPROMELLOSE 2910 (5 MPA.S)

Code: R75537T0T4

Class Code: IACT

POVIDONE K30

Code: U725QWY32X

Class Code: IACT

POLYETHYLENE GLYCOL 400

Code: B697894SGQ

Class Code: IACT

SODIUM STARCH GLYCOLATE TYPE A POTATO

Code: 5856J3G2A2

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

Active Moieties

Code: 5E8K9I0O4U

Ciprofloxacin

Basic Information

Regulatory Information

Company Information

Active Ingredients

SILICON DIOXIDE

MICROCRYSTALLINE CELLULOSE

HYPROMELLOSE 2910 (5 MPA.S)

POVIDONE K30

POLYETHYLENE GLYCOL 400

SODIUM STARCH GLYCOLATE TYPE A POTATO

TITANIUM DIOXIDE

MAGNESIUM STEARATE

Active Moieties

CIPROFLOXACIN