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: 63187-250
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)
Microcrystalline cellulose ( UNII: OP1R32D61U)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Sodium starch glycolate type a potato ( UNII: 5856J3G2A2)
Magnesium stearate ( UNII: 70097M6I30)
Hypromellose, unspecified ( UNII: 3NXW29V3WO)
Talc ( UNII: 7SEV7J4R1U)
Titanium dioxide ( UNII: 15FIX9V2JP)
Polyethylene glycol, unspecified ( UNII: 3WJQ0SDW1A)
Water ( UNII: 059QF0KO0R)

Product Characteristics

Color WHITE (WHITE) Size 6 mm
Shape CAPSULE (CAPSULE) Score 1
Imprint Code WW928

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA076558 USA

Labeler - Proficient Rx LP( 079196022)

Establishment

Name ID/FEI Business Operations
Proficient Rx LP 079196022 REPACK( 63187-250), RELABEL( 63187-250)