Olanzapine (Page 12 of 12)

PRINCIPAL DISPLAY PANEL – 5 MG

Carton-5 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 10 MG

Carton-10 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 15 MG

Carton-15 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 20 MG

Carton-20 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL – BLISTERS – 5 MG

Blister-5 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL – BLISTERS — 10 MG

Blister-10 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL – BLISTERS – 15 MG

Blister-15 mg
(click image for full-size original)

PRINCIPAL DISPLAY PANEL – BLISTERS – 20 MG

Blister- 20 mg
(click image for full-size original)

OLANZAPINE olanzapine tablet, orally disintegrating
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:49884-320
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OLANZAPINE (OLANZAPINE) OLANZAPINE 5 mg
Inactive Ingredients
Ingredient Name Strength
MAGNESIUM SULFATE, UNSPECIFIED
Product Characteristics
Color yellow Score no score
Shape ROUND Size 6mm
Flavor PINEAPPLE Imprint Code P;320
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49884-320-55 3 BLISTER PACK in 1 CARTON contains a BLISTER PACK (49884-320-52)
1 NDC:49884-320-52 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK This package is contained within the CARTON (49884-320-55)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078109 10/24/2011
OLANZAPINE olanzapine tablet, orally disintegrating
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:49884-321
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OLANZAPINE (OLANZAPINE) OLANZAPINE 10 mg
Inactive Ingredients
Ingredient Name Strength
MAGNESIUM SULFATE, UNSPECIFIED
Product Characteristics
Color yellow Score no score
Shape ROUND Size 8mm
Flavor PINEAPPLE Imprint Code P;321
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49884-321-55 3 BLISTER PACK in 1 CARTON contains a BLISTER PACK (49884-321-52)
1 NDC:49884-321-52 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK This package is contained within the CARTON (49884-321-55)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078109 10/24/2011
OLANZAPINE olanzapine tablet, orally disintegrating
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:49884-322
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OLANZAPINE (OLANZAPINE) OLANZAPINE 15 mg
Inactive Ingredients
Ingredient Name Strength
MAGNESIUM SULFATE, UNSPECIFIED
Product Characteristics
Color yellow Score no score
Shape ROUND Size 10mm
Flavor PINEAPPLE Imprint Code P;322
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49884-322-55 3 BLISTER PACK in 1 CARTON contains a BLISTER PACK (49884-322-52)
1 NDC:49884-322-52 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK This package is contained within the CARTON (49884-322-55)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078109 10/24/2011
OLANZAPINE olanzapine tablet, orally disintegrating
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:49884-323
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OLANZAPINE (OLANZAPINE) OLANZAPINE 20 mg
Inactive Ingredients
Ingredient Name Strength
MAGNESIUM SULFATE, UNSPECIFIED
Product Characteristics
Color yellow Score no score
Shape ROUND Size 12mm
Flavor PINEAPPLE Imprint Code P;323
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49884-323-55 3 BLISTER PACK in 1 CARTON contains a BLISTER PACK (49884-323-52)
1 NDC:49884-323-52 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK This package is contained within the CARTON (49884-323-55)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078109 10/24/2011
Labeler — Par Pharmaceutical, Inc. (092733690)

Revised: 07/2021 Par Pharmaceutical, Inc.

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