NDC 67046-522

Olanzapine

Olanzapine

Olanzapine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Olanzapine.

Product ID67046-522_5a1dc228-b758-5f2b-e053-2991aa0adccc
NDC67046-522
Product TypeHuman Prescription Drug
Proprietary NameOlanzapine
Generic NameOlanzapine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-09-26
Marketing CategoryANDA / ANDA
Application NumberANDA090798
Labeler NameContract Pharmacy Services-PA
Substance NameOLANZAPINE
Active Ingredient Strength5 mg/1
Pharm ClassesAtypical Antipsychotic [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 67046-522-60

60 TABLET, FILM COATED in 1 BLISTER PACK (67046-522-60)
Marketing Start Date2017-09-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-522-21 [67046052221]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-15 [67046052215]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-30 [67046052230]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-14 [67046052214]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-20 [67046052220]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-28 [67046052228]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-07 [67046052207]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

NDC 67046-522-60 [67046052260]

Olanzapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090798
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
OLANZAPINE5 mg/1

OpenFDA Data

SPL SET ID:5a1dc228-b757-5f2b-e053-2991aa0adccc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312078
  • 312077
    • UPC Code
  • 0360505311187
  • 0360505311484

    • Pharmacological Class

    • Atypical Antipsychotic [EPC]

    NDC Crossover Matching brand name "Olanzapine" or generic name "Olanzapine"

    NDCBrand NameGeneric Name
    67877-175OlanzapineOlanzapine
    67877-174OlanzapineOlanzapine
    67877-172OlanzapineOlanzapine
    67877-173OlanzapineOlanzapine
    67877-176OlanzapineOlanzapine
    67877-177OlanzapineOlanzapine
    68084-529OlanzapineOlanzapine
    68084-723OlanzapineOlanzapine
    68084-528OlanzapineOlanzapine
    68084-740OlanzapineOlanzapine
    68084-525OlanzapineOlanzapine
    68258-7095OlanzapineOlanzapine
    68258-7152OlanzapineOlanzapine
    68258-7153OlanzapineOlanzapine
    68258-7154OlanzapineOlanzapine
    68382-365olanzapineolanzapine
    68382-368olanzapineolanzapine
    68258-7096OlanzapineOlanzapine
    68382-367olanzapineolanzapine
    68382-364olanzapineolanzapine
    68382-366olanzapineolanzapine
    68382-369olanzapineolanzapine
    68788-7161OlanzapineOlanzapine
    0517-0955OlanzapineOlanzapine
    69189-5510OlanzapineOlanzapine
    69543-384OlanzapineOlanzapine
    69543-380OlanzapineOlanzapine
    69543-381OlanzapineOlanzapine
    69543-383OlanzapineOlanzapine
    69543-382OlanzapineOlanzapine
    69543-385OlanzapineOlanzapine
    69807-2012OlanzapineOlanzapine
    69807-2011OlanzapineOlanzapine
    69807-2013OlanzapineOlanzapine
    70518-0026OlanzapineOlanzapine
    70518-0148OlanzapineOlanzapine
    70518-0145OlanzapineOlanzapine
    70518-0149OlanzapineOlanzapine
    70518-0314OlanzapineOlanzapine
    70518-0477OlanzapineOlanzapine
    70518-0110OlanzapineOlanzapine
    70518-0616OlanzapineOlanzapine
    70518-0144OlanzapineOlanzapine
    70518-0433OlanzapineOlanzapine
    70518-1206OlanzapineOlanzapine
    70518-0921OlanzapineOlanzapine
    70518-1207OlanzapineOlanzapine
    70518-0615OlanzapineOlanzapine
    70518-1115OlanzapineOlanzapine
    70518-1154OlanzapineOlanzapine
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