Product Images Diclofenac Sodium

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Product Label Images

The following 11 images provide visual information about the product associated with Diclofenac Sodium NDC 70748-335 by Lupin Pharmaceuticals, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Figure 1 - 6710e1e8 7999 4015 b695 3bb550be114b 01

Figure 1 - 6710e1e8 7999 4015 b695 3bb550be114b 01

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Figure A - 6710e1e8 7999 4015 b695 3bb550be114b 07

Figure A - 6710e1e8 7999 4015 b695 3bb550be114b 07

Figure B - 6710e1e8 7999 4015 b695 3bb550be114b 08

Figure B - 6710e1e8 7999 4015 b695 3bb550be114b 08

Figure C and D - 6710e1e8 7999 4015 b695 3bb550be114b 09

Figure C and D - 6710e1e8 7999 4015 b695 3bb550be114b 09

Bottle Label - 6710e1e8 7999 4015 b695 3bb550be114b 10

Bottle Label - 6710e1e8 7999 4015 b695 3bb550be114b 10

NDC 70748-335-01 is a Diclofenac Sodium Topical Solution used for external use only to relieve pain caused by osteoarthritis of the knees. Each pump actuation delivers 1 gram of solution containing 20 mg diclofenac sodium. Users should apply two pump activations on their affected knee(s) twice a day. The medication guide enclosed with the product should be dispensed to each patient. The product must be stored at 25°C (77°F), with allowable excursions between 15°C to 30°C (59°F to 86°F) per USP Controlled Room Temperature. Distributed by Lupin Pharmaceuticals Inc. in Baltimore, Maryland.*

Carton Label - 6710e1e8 7999 4015 b695 3bb550be114b 11

Carton Label - 6710e1e8 7999 4015 b695 3bb550be114b 11

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.