Atomoxetine Capsule
Product Images NDC 68462-271

11 FDA label images from Glenmark Pharmaceuticals Inc., Usa · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Atomoxetine (NDC 68462-271). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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

Figure1 (Figure1)

Figure1 (Figure1)
Two line graphs showing mean weight percentile and mean height percentile over 36 months of treatment. The left graph depicts mean weight percentile for 203 subjects, showing fluctuations and a gradual increase. The right graph illustrates mean height percentile for 155 subjects, with relatively stable values and slight variation over time.*
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Structure (Structure)

Structure (Structure)
Chemical structure of atomoxetine hydrochloride, showing its molecular arrangement including aromatic rings, a methyl group, and an amine linked to a hydrochloride component.*
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Logo1 (Logo1)

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Logo2 (Logo2)

FDA Label Image

10mg-label (10mg Label)

10mg-label (10mg Label)
Label for Atomoxetine Capsules, USP 10 mg by Glenmark Pharmaceuticals Inc., USA. The label indicates prescription-only status, contains 30 capsules, and includes storage instructions. It features the NDC 68462-265-30 and contact information for the manufacturer along with a Medication Guide URL.*
FDA Label Image

18mg-label (18mg Label)

18mg-label (18mg Label)
Atomoxetine Capsules, USP 18 mg oral capsules package label from Glenmark Pharmaceuticals Inc., USA. The label shows the NDC 68462-266-30 and indicates the product contains 30 capsules. It includes directions to dispense an enclosed Medication Guide and a barcode.*
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25mg-label (25mg Label)

25mg-label (25mg Label)
Label for atomoxetine capsules, USP 25 mg strength, in a bottle containing 30 capsules. The label includes the NDC 68462-267-30 and indicates it is distributed by Glenmark Pharmaceuticals Inc., USA. Storage instructions, a barcode, and a contact number for questions are also visible.*
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40mg-label (40mg Label)

40mg-label (40mg Label)
Label for Atomoxetine Capsules, USP 40 mg oral capsules by Glenmark Pharmaceuticals Inc., USA. The label shows NDC 68462-268-30, a 30-capsule prescription package. It includes usage instructions, storage conditions (20° to 25°C), pharmacist dispensing guidance, and contact information for Glenmark Pharmaceuticals.*
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60mg-label (60mg Label)

60mg-label (60mg Label)
Label for atomoxetine capsules USP 60 mg by Glenmark Pharmaceuticals Inc., USA. The label states the NDC number 68462-269-30 and indicates the package contains 30 capsules. It includes storage instructions, pharmacist dispensing information, and contact details for Glenmark Pharmaceuticals.*
FDA Label Image

80mg-label (80mg Label)

80mg-label (80mg Label)
Label for Atomoxetine Capsules USP 80 mg by Glenmark Pharmaceuticals Inc., USA. The label indicates the product contains 30 capsules for oral use. It includes storage instructions, a note to pharmacists to dispense the Medication Guide to patients, and contact information for Glenmark Pharmaceuticals. The NDC number is 68462-270-30.*
FDA Label Image

100mg-label (100mg Label)

100mg-label (100mg Label)
The label for atomoxetine capsules, USP, shows a 100 mg dosage strength. The product is from Glenmark Pharmaceuticals Inc., USA, and the package contains 30 capsules for oral use. The label includes the NDC number 68462-271-30 and instructions for pharmacists to dispense the enclosed medication guide to each patient.*

* 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.