60505-3114 : Olanzapine 15 mg Oral Tablet

NDC:	60505-3114
Labeler:	Apotex Corp.
Product Type:	Human Prescription Drug
Drug Name:	Olanzapine
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA090798
Rev. Date:	Apr 23, 2012

Appearance:

Markings:	APO;OLA;15
Shapes:	Oval
Colors:	Blue
Size (mm):	12
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

APO OLA 15: (60505-3114) Olanzapine 15 mg Oral Tablet by Apotex Corp.

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

60505-3114-0: 10 BLISTER PACK IN 1 CARTON (60505‑3114‑0) > 10 TABLET, FILM COATED IN 1 BLISTER PACK
60505-3114-3: 30 TABLET, FILM COATED IN 1 BOTTLE (60505‑3114‑3)
60505-3114-8: 1000 TABLET, FILM COATED IN 1 BOTTLE (60505‑3114‑8)

Active Ingredients:

Olanzapine

Dosage Strength:

15 mg

Inactive Ingredients:

Lactose Monohydrate
Cellulose, Microcrystalline
Starch, Corn
Hypromellose 2910 (6 Mpa.s)
Magnesium Stearate
Hydroxypropyl Cellulose
Polyethylene Glycol
Titanium Dioxide
Fd&c Blue No. 2

Pharmaceutical Classes:

Atypical Antipsychotic [EPC]

NDC QR Code

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NDC 60505-3114 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.