Olanzapine Tablet
Product Images NDC 71209-077

Product Visual Gallery

This gallery contains 25 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 71209-077). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cadila 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

Olanzapine-spl-strc (Olanzapine Spl Strc)

Chemical structure of olanzapine, a compound characterized by fused aromatic rings including a thiophene and piperazine ring, with methyl substitutions.*

FDA Label Image

Cont-label-30s-2-5mg (Cont Label 30s 2 5mg)

Label for Olanzapine Tablets USP 2.5 mg oral tablets, manufactured by Cadila Pharmaceuticals Limited. The label states storage instructions, prescription requirements, and package size of 30 tablets. It includes warnings to keep out of reach of children and dispensing instructions for pharmacists. NDC number 71209-073-01 is visible along with a barcode.*

FDA Label Image

Cont-label-100s-2-5-mg (Cont Label 100s 2 5 mg)

Label for Olanzapine Tablets USP 2.5 mg oral tablets by Cadila Pharmaceuticals Limited. The label includes storage instructions, a NDC number (71209-073-05), a note to pharmacists to dispense the Medication Guide, and packaging details for 100 tablets. The product is manufactured in Gujarat, India.*

FDA Label Image

Cont-label-500s-2-5mg (Cont Label 500s 2 5mg)

Olanzapine Tablets USP 2.5 mg film-coated oral tablets packaging label. The label includes storage instructions, manufacturer Cadila Pharmaceuticals Ltd. Gujarat, India, and states the package contains 500 tablets. The label includes a barcode and notes dispensing with Medication Guide.*

FDA Label Image

Cont-label-1000s-2-5mg (Cont Label 1000s 2 5mg)

Olanzapine Tablets USP 2.5 mg film-coated tablets label from Cadila Pharmaceuticals Limited. The label includes dosage strength, NDC 71209-073-11, storage instructions, pharmacist directions to dispense the Medication Guide, and packaging for 1000 tablets. Manufactured in Gujarat, India, with a barcode and specified storage conditions.*

FDA Label Image

Cont-label-30s-5mg (Cont Label 30s 5mg)

Olanzapine Tablets USP 5 mg film-coated tablets label from Cadila Pharmaceuticals Limited. The label includes dosage strength 5 mg, package quantity of 30 tablets, and instructions to dispense the medication guide to patients. Storage and safety instructions are also visible along with the NDC code 71209-074-01.*

FDA Label Image

Cont-label-100s-5mg (Cont Label 100s 5mg)

Olanzapine Tablets USP 5 mg oral tablets packaging label displays the proprietary name, dosage strength, and quantity of 100 tablets. It includes storage instructions at 25°C, a caution to keep out of reach of children, and is manufactured by Cadila Pharmaceuticals Limited, Gujarat, India. The label also features a barcode and a warning that it is Rx only.*

FDA Label Image

Cont-label-500s-5mg (Cont Label 500s 5mg)

Label for Olanzapine Tablets, USP 5 mg, showing a film-coated oral tablet product by Cadila Pharmaceuticals Ltd. The label includes the NDC number 71209-074-10, instructions for storage and dispensing, barcode, and an indication that the package contains 500 tablets. It also highlights pharmacist dispensing information and a note for serialized datamatrix coding space.*

FDA Label Image

Cont-label-1000s-5mg (Cont Label 1000s 5mg)

Olanzapine Tablets, USP 5 mg oral tablets packaging label displaying the product name and strength prominently, manufactured by Cadila Pharmaceuticals Limited. The label states a package count of 1000 tablets with a prescription-only designation. Storage instructions, a caution to keep out of children's reach, and pharmacist dispensing guidance are also visible.*

FDA Label Image

Cont-label-30s-7-5mg (Cont Label 30s 7 5mg)

Packaging label for Olanzapine Tablets USP, 7.5 mg oral tablets by Cadila Pharmaceuticals Limited. The label indicates a 30-tablet count with prescription only (Rx only). Storage instructions and a notation to dispense the Medication Guide to each patient are included. The label also contains a barcode and manufacturer information from Gujarat, India.*

FDA Label Image

Cont-label-100s-7-5-mg (Cont Label 100s 7 5 mg)

Label for Olanzapine Tablets, USP 7.5 mg oral tablets, manufactured by Cadila Pharmaceuticals Limited. The label shows storage instructions, dosage strength, a note to dispense the accompanying Medication Guide, and a package count of 100 tablets. It includes the NDC number 71209-075-05 and manufacturer location in Gujarat, India.*

FDA Label Image

Cont-label-500s-7-5mg (Cont Label 500s 7 5mg)

Label for Olanzapine Tablets USP, 7.5 mg oral tablets by Cadila Pharmaceuticals Limited. The label indicates a 500-tablet quantity and includes storage instructions, dosage strength, NDC 71209-075-10, and a barcode. It features a warning to keep medication out of children's reach and instructions for pharmacists to dispense the Medication Guide.*

FDA Label Image

Cont-label-1000s-7-5mg (Cont Label 1000s 7 5mg)

Olanzapine Tablets, USP 7.5 mg oral tablets in a package of 1000 tablets, manufactured by Cadila Pharmaceuticals Limited, Gujarat, India. The label includes storage instructions, a barcode, and a prescription-only designation. The NDC is 71209-075-11.*

FDA Label Image

Cont-label-30s-10mg (Cont Label 30s 10mg)

Olanzapine Tablets USP 10 mg film-coated tablets label from Cadila Pharmaceuticals Limited. The label includes storage instructions, a warning to keep out of reach of children, prescription status (Rx only), and indicates a package of 30 tablets. It also features an NDC barcode and pharmacist guidance for dispensing the Medication Guide.*

FDA Label Image

Cont-label-100s-10mg (Cont Label 100s 10mg)

Label for Olanzapine Tablets, USP 10 mg oral tablets by Cadila Pharmaceuticals Limited. The label specifies 100 tablets per container, includes storage instructions at 25°C with permitted excursions, and advises dispensing with the Medication Guide. The label also emphasizes keeping medication out of children’s reach and has a barcode with NDC 71209-076-05.*

FDA Label Image

Cont-label-500s-10-mg (Cont Label 500s 10 mg)

Olanzapine Tablets, USP 10 mg film-coated oral tablets label by Cadila Pharmaceuticals Limited. The label states the product contains olanzapine 10 mg per tablet, with packaging for 500 tablets. It includes storage instructions, pharmacist dispensing guidance, and a barcode. Manufactured in Gujarat, India.*

FDA Label Image

Cont-label-1000s-10-mg (Cont Label 1000s 10 mg)

Olanzapine Tablets USP 10 mg film-coated tablets. The label includes storage instructions, pharmacist dispensing guidance, and safety warnings. The product is manufactured by Cadila Pharmaceuticals Limited, Gujarat, India. The package contains 1000 tablets, labeled Rx only, and features a barcode and the NDC number 71209-076-11.*

FDA Label Image

Cont-label-30s-15mg (Cont Label 30s 15mg)

Olanzapine Tablets, USP 15 mg film-coated tablets label from Cadila Pharmaceuticals Limited. The label includes storage instructions, warnings to keep out of reach of children, pharmacist dispensing guidance, and indicates a package containing 30 tablets. Batch coding and serialization space is noted for a 44 x 25 mm area.*

FDA Label Image

Cont-label-100s-15mg (Cont Label 100s 15mg)

Olanzapine Tablets USP 15 mg oral film-coated tablets packaging label. The label includes instructions for storage, dispensing, and safety warnings. It indicates the product is manufactured by Cadila Pharmaceuticals Ltd., Gujarat, India, and comes in a bottle containing 100 tablets. The label features the NDC 71209-077-05 and a barcode.*

FDA Label Image

Cont-label-500s-15mg (Cont Label 500s 15mg)

Olanzapine Tablets, USP 15 mg oral tablets label from Cadila Pharmaceuticals Limited. The label states the product contains 500 tablets, includes a barcode, NDC 71209-077-10, and storage instructions specifying controlled room temperature. It also highlights pharmacist instructions and warnings such as keeping medications out of children's reach.*

FDA Label Image

Cont-label-1000s-15mg (Cont Label 1000s 15mg)

Olanzapine Tablets, USP 15 mg film-coated tablets label by Cadila Pharmaceuticals Ltd. The label states storage instructions, pharmacist dispensing information, and packaging of 1000 tablets. The NDC number is 71209-077-11. The label includes a barcode and a note about the unvarnished area for datamatrix coding.*

FDA Label Image

Cont-label-30s-20mg (Cont Label 30s 20mg)

Label for Olanzapine Tablets, USP 20 mg by Cadila Pharmaceuticals Limited. It is a film-coated oral tablet available in a package containing 30 tablets. The label includes dosage strength, storage instructions, manufacturer details, and pharmacy dispensing information, along with an NDC code and barcode.*

FDA Label Image

Cont-label-100s-20mg (Cont Label 100s 20mg)

Label for Olanzapine Tablets, USP 20 mg oral tablets. The label states each film-coated tablet contains 20 mg olanzapine. It includes storage instructions (25°C with permitted excursions), a warning to keep out of children's reach, and mentions dispensing with a Medication Guide. The label also shows the NDC number 71209-078-05, a barcode, quantity of 100 tablets, and manufacturer as Cadila Pharmaceuticals Ltd., Gujarat, India.*

FDA Label Image

Cont-label-500s-20mg (Cont Label 500s 20mg)

Label for Olanzapine Tablets, USP 20 mg by Cadila Pharmaceuticals Limited. The label states the tablet strength as 20 mg, includes storage instructions, dosage note to see prescribing information, and a warning to keep medication out of children's reach. It also indicates the package contains 500 tablets with 'Rx only' and includes a barcode.*

FDA Label Image

Cont-label-1000s-20mg (Cont Label 1000s 20mg)

Label for Olanzapine Tablets, USP 20 mg, manufactured by Cadila Pharmaceuticals Limited. This oral tablet packaging contains 1000 tablets. The label includes storage instructions, a barcode, and a prominent dosage strength display in a maroon box. It also notes prescription-only status and pharmacist dispensing guidance.*

* 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.