Ciprofloxacin (Page 14 of 14)

Ciprofloxacin 250 mg

Ciprofloxacin 250 mg
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CIPROFLOXACIN ciprofloxacin hydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63739-700(NDC:16714-651)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CIPROFLOXACIN HYDROCHLORIDE (CIPROFLOXACIN) CIPROFLOXACIN 250 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE
SODIUM STARCH GLYCOLATE TYPE A POTATO
POVIDONE K30
SILICON DIOXIDE
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (5 MPA.S)
POLYETHYLENE GLYCOL 400
TITANIUM DIOXIDE
Product Characteristics
Color white (White to Off-white) Score no score
Shape ROUND Size 11mm
Flavor Imprint Code C;95
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63739-700-10 10 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK
1 10 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (63739-700-10)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077859 04/26/2007
Labeler — Mckesson Corporation DBA SKY Packaginng (140529962)

Revised: 01/2023 Mckesson Corporation DBA SKY Packaginng

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