Ofloxacin (Page 10 of 10)

Package/Label Display Panel

Ofloxacin Tablets 200 mg, 100s Label
(click image for full-size original)

Ofloxacin Tablets 200 mg, 100s Label Text

NDC 0093-7180 -01

OFLOXACIN
Tablets
200 mg

PHARMACIST: Dispense the accompanying
Medication Guide to each patient.

Rx only

100 TABLETS

TEVA

Package/Label Display Panel

Ofloxacin Tablets 300 mg, 100s Label
(click image for full-size original)

Ofloxacin Tablets 300 mg, 100s Label Text

NDC 0093-7181 -01

OFLOXACIN
Tablets
300 mg

PHARMACIST: Dispense the accompanying
Medication Guide to each patient.

Rx only

100 TABLETS

TEVA

Package/Label Display Panel

Ofloxacin Tablets 400 mg, 100s Label
(click image for full-size original)

Ofloxacin Tablets 400 mg, 100s Label Text

NDC 0093-7182 -01

OFLOXACIN
Tablets
400 mg

PHARMACIST: Dispense the accompanying
Medication Guide to each patient.

Rx only

100 TABLETS

TEVA

OFLOXACIN
ofloxacin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0093-7180
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OFLOXACIN (OFLOXACIN) OFLOXACIN 200 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
HYDROXYPROPYL CELLULOSE (TYPE H)
HYPROMELLOSE 2910 (3 MPA.S)
HYPROMELLOSE 2910 (5 MPA.S)
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL 400
POLYSORBATE 80
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
Product Characteristics
Color YELLOW (light-yellow) Score no score
Shape OVAL (oval-shaped) Size 15mm
Flavor Imprint Code 93;7180
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0093-7180-01 100 TABLET, FILM COATED in 1 BOTTLE None
Image of Product
(click image for full-size original)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076182 01/28/2004 03/31/2015
OFLOXACIN
ofloxacin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0093-7181
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OFLOXACIN (OFLOXACIN) OFLOXACIN 300 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
HYDROXYPROPYL CELLULOSE (TYPE H)
HYPROMELLOSE 2910 (3 MPA.S)
HYPROMELLOSE 2910 (5 MPA.S)
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL 400
POLYSORBATE 80
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape OVAL (oval-shaped) Size 17mm
Flavor Imprint Code 93;7181
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0093-7181-01 100 TABLET, FILM COATED in 1 BOTTLE None
Image of Product
(click image for full-size original)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076182 01/28/2004 07/31/2015
OFLOXACIN
ofloxacin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0093-7182
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OFLOXACIN (OFLOXACIN) OFLOXACIN 400 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
HYDROXYPROPYL CELLULOSE (TYPE H)
HYPROMELLOSE 2910 (3 MPA.S)
HYPROMELLOSE 2910 (5 MPA.S)
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL 400
POLYSORBATE 80
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
FERRIC OXIDE RED
Product Characteristics
Color YELLOW (pale-gold) Score no score
Shape OVAL (oval-shaped) Size 18mm
Flavor Imprint Code 93;7182
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0093-7182-01 100 TABLET, FILM COATED in 1 BOTTLE None
Image of Product
(click image for full-size original)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076182 01/28/2004 07/31/2015
Labeler — Teva Pharmaceuticals USA Inc (001627975)

Revised: 12/2014 Teva Pharmaceuticals USA Inc

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