Ciprofloxacin (Page 15 of 15)

NDC 0143-9927-01
Ciprofloxacin Tablets, USP
250 mg
100 TabletsRx Only

Ciprofloxacin--250mg-100-tabs
(click image for full-size original)

NDC 0143-9928-01
Ciprofloxacin Tablets, USP
500 mg
100 TabletsRx Only

Ciprofloxacin-500mg-100-tabs
(click image for full-size original)

NDC 0143-9929-50
Ciprofloxacin Tablets, USP
750 mg
50 TabletsRx Only

Ciprofloxacin-750-mg-100-tabs
(click image for full-size original)
CIPROFLOXACIN ciprofloxacin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0143-9927
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
SILICON DIOXIDE
STARCH, CORN
CORN OIL
HYPROMELLOSES
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYETHYLENE GLYCOL, UNSPECIFIED
WATER
SODIUM STARCH GLYCOLATE TYPE A POTATO
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape ROUND Size 10mm
Flavor Imprint Code WW927
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0143-9927-01 100 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:0143-9927-05 500 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:0143-9927-30 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076558 06/09/2004
CIPROFLOXACIN ciprofloxacin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0143-9928
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CIPROFLOXACIN HYDROCHLORIDE (CIPROFLOXACIN) CIPROFLOXACIN 500 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
STARCH, CORN
CORN OIL
HYPROMELLOSES
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYETHYLENE GLYCOL, UNSPECIFIED
WATER
SODIUM STARCH GLYCOLATE TYPE A POTATO
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape CAPSULE Size 11mm
Flavor Imprint Code WW928
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0143-9928-01 100 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:0143-9928-05 500 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:0143-9928-30 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076558 06/09/2004
CIPROFLOXACIN ciprofloxacin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0143-9929
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CIPROFLOXACIN HYDROCHLORIDE (CIPROFLOXACIN) CIPROFLOXACIN 750 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
STARCH, CORN
CORN OIL
HYPROMELLOSES
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYETHYLENE GLYCOL, UNSPECIFIED
WATER
SODIUM STARCH GLYCOLATE TYPE A POTATO
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape CAPSULE Size 11mm
Flavor Imprint Code WW929
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0143-9929-01 100 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:0143-9929-50 50 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076558 06/09/2004
Labeler — Hikma Pharmaceuticals USA Inc. (001230762)

Revised: 12/2022 Hikma Pharmaceuticals USA Inc.

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