Ciprofloxacin tablet, film coated

Ingredients and appearance - Product information

Ciprofloxacin tablet, film coated- Ciprofloxacin

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 42708-002
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Ciprofloxacin hydrochloride ( UNII: 4BA73M5E37)( Ciprofloxacin - UNII: 5E8K9I0O4U ) 500 mgin 1

Inactive Ingredients

Ingredient Name Code
Starch, corn ( UNII: O8232NY3SJ)
Crospovidone, unspecified ( UNII: 2S7830E561)
Magnesium stearate ( UNII: 70097M6I30)
Microcrystalline cellulose ( UNII: OP1R32D61U)
Polyethylene glycol, unspecified ( UNII: 3WJQ0SDW1A)
Polyvinyl alcohol, unspecified ( UNII: 532B59J990)
Water ( UNII: 059QF0KO0R)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Talc ( UNII: 7SEV7J4R1U)
Titanium dioxide ( UNII: 15FIX9V2JP)

Product Characteristics

Color WHITE (White to off-white) Size 18 mm
Shape OVAL (capsule shaped) Score 1
Imprint Code CR;500

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA076794 USA

Labeler - QPharma Inc( 030620888)

Establishment

Name ID/FEI Business Operations
QPharma Inc 030620888 REPACK( 42708-002)