Ciprofloxacin tablet

Ingredients and appearance - Product information

Ciprofloxacin tablet- Ciprofloxacin

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 61919-735
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Ciprofloxacin hydrochloride ( UNII: 4BA73M5E37)( Ciprofloxacin - UNII: 5E8K9I0O4U ) 750 mgin 1

Inactive Ingredients

Ingredient Name Code
Cellulose, microcrystalline ( UNII: OP1R32D61U)
Titanium dioxide ( UNII: 15FIX9V2JP)
Polyethylene glycols ( UNII: 3WJQ0SDW1A)
Hypromelloses ( UNII: 3NXW29V3WO)
Starch, corn ( UNII: O8232NY3SJ)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Crospovidone (15 mpa.s at 5%) ( UNII: 68401960MK)
Magnesium stearate ( UNII: 70097M6I30)
Water ( UNII: 059QF0KO0R)

Product Characteristics

Shape CAPSULE Score
Imprint Code P;750 Color white (white (white to slightly yellowish))
Size 23 mm

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 61919-735-90 90 in 1 BOTTLE 2016/09/12

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA076639 USA 2016/09/12

Labeler - DIRECT RX( 079254320)

Establishment

Name ID/FEI Business Operations
DIRECT RX 079254320 repack( 61919-735)