Olanzapine Tablet, Orally Disintegrating
Product Images NDC 13668-088

13 FDA label images from Torrent Pharmaceuticals Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 13668-088). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Torrent Pharmaceuticals Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Str (Fa37d6c9 F803 4efc 8789 4095824eb63e 01)

Str (Fa37d6c9 F803 4efc 8789 4095824eb63e 01)
Chemical structure diagram of olanzapine, showing its molecular configuration with heterocyclic rings and attached functional groups.*
FDA Label Image

Logo (Fa37d6c9 F803 4efc 8789 4095824eb63e 02)

FDA Label Image

Tpl Logo (Fa37d6c9 F803 4efc 8789 4095824eb63e 03)

FDA Label Image

2.5 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 04)

2.5 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 04)
Olanzapine Tablets, USP 2.5 mg orally disintegrating tablets label by Torrent Pharmaceuticals Limited. The label shows a package containing 30 tablets, includes storage instructions, prescription status (Rx only), and directions for pharmacists to dispense the accompanying medication guide. The label includes barcodes and manufacturing information for Torrent Pharma Inc., Levittown, PA.*
FDA Label Image

5 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 05)

5 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 05)
Olanzapine Tablets, USP 5 mg orally disintegrating tablets packaging label by Torrent Pharmaceuticals Limited. The label indicates a bottle containing 30 tablets with NDC 13668-167-30. It includes storage instructions, pharmacist dispensing directions, and a barcode.*
FDA Label Image

7.5 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 06)

7.5 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 06)
Olanzapine Tablets, USP 7.5 mg orally disintegrating tablets label with packaging for 30 tablets. The label includes dosage strength, storage instructions, manufacturer Torrent Pharmaceuticals Limited, and the NDC 13668-168-30. The label notes the product is prescription-only (Rx only).*
FDA Label Image

10 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 07)

10  mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 07)
Label for Olanzapine Tablets, USP 10 mg, 30 tablets per bottle. Orally disintegrating tablets manufactured by Torrent Pharmaceuticals Ltd., India, and labeled for Torrent Pharma Inc., Levittown, PA. Label includes storage instructions, a barcode, and a note to dispense with accompanying Medication Guide. NDC 13668-169-30 is printed on the label.*
FDA Label Image

15 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 08)

15 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 08)
Label for Olanzapine Tablets USP 15 mg, 30 tablets per container, marked Rx only. Manufactured by Torrent Pharmaceuticals Limited in India and for Torrent Pharma Inc., Levittown, PA. Storage instructions specify maintaining 20° to 25°C with permitted excursions. Label includes barcode, NDC 13668-170-30, and guidance to pharmacists to dispense accompanying Medication Guide.*
FDA Label Image

20 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 09)

20 mg, Tablet (Fa37d6c9 F803 4efc 8789 4095824eb63e 09)
Olanzapine Tablets, USP 20 mg, orally disintegrating tablets package containing 30 tablets. The label shows storage instructions, prescribing information notice, and is marked Rx only. Manufactured by Torrent Pharmaceuticals Ltd., India, and for Torrent Pharma Inc., Levittown, PA. The label features the NDC 13668-171-30 and a barcode.*
FDA Label Image

5 mg Orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 10)

5 mg Orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 10)
Label for Olanzapine Orally Disintegrating Tablets, USP, 5 mg strength in a package of 30 tablets. Manufactured by Torrent Pharmaceuticals Limited. The label includes storage instructions, phenylketonurics warning, and pharmacist dispensing information. The label bears the NDC code 13668-086-30 and is marked Rx only.*
FDA Label Image

10 mg, Orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 11)

10 mg, Orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 11)
Label for Olanzapine Orally Disintegrating Tablets, USP 10 mg, with a count of 30 tablets. The label includes storage instructions, phenylalanine content, and dispensing guidance. It is manufactured by Torrent Pharmaceuticals Limited and labeled for prescription use only. The label also features a barcode and the NDC number 13668-088-30.*
FDA Label Image

15 mg, Orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 12)

15 mg, Orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 12)
The packaging label for Olanzapine Orally Disintegrating Tablets, USP, 15 mg strength, contains 30 tablets. The label shows the NDC number 13668-089-30 and includes storage instructions, dosage information, and a warning for phenylketonurics about phenylalanine content. It is manufactured by Torrent Pharmaceuticals Limited and labeled for Rx only use. The label also advises dispensing the accompanying Medication Guide to patients.*
FDA Label Image

20 mg,orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 13)

20 mg,orally Disintegrating Tablets (Fa37d6c9 F803 4efc 8789 4095824eb63e 13)
Label for Olanzapine Orally Disintegrating Tablets USP, 20 mg, containing 30 tablets. The label includes storage instructions, phenylalanine content warning, and manufacturer details (Torrent Pharmaceuticals Ltd). It states the product is Rx only and features the Torrent Pharma logo and an NDC code 13668-090-30.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.