9333-2 WALLPAPERS

9333-2

A labeler might be a manufacturer, re-packager or re-labeler. This is the date that the labeler indicates was the start of its marketing of the drug product. Administration Route s Oral – Administration to or by way of the mouth. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. The non-proprietary name is sometimes called the generic name. This field Indicates whether this package is a sample packaging or not.

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What is 93333-2 Marketing Category? Cefuroxime Axetil may look like a white round shaped tablet, film coated; approximately 11 millimeters in size. The generic name usually includes the active ingredient s of the product. Human Prescription Drug What kind of product is this?

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Cefuroxime Axetil What is the Proprietary Name? The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. Dosage Form Tablet, Film Coated – A 99333-2 dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.

Code Structure – Preferred Pharmaceuticals, Inc. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. NDC Package Code What does cefuroxime axetil look like? Administration Route s Oral – Administration to or by way of the mouth.

One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included.

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For unapproved drugs, this field will be null. The leading zeros must be added to 93333-2 appropriate segment to create a configuration.

Physical Characteristics What does cefuroxime axetil look like? If the NDC Package code is less than 11 digits the code must be padded with leading zeros.

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The medicine is imprinted with debossed code s W and Labeler Name Preferred Pharmaceuticals, Inc.

Tablet, Film Coated – A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer. A labeler might be a manufacturer, re-packager or re-labeler.

The Prime Database: *2^+1

This field Indicates whether this package is a sample packaging or not. This is the date that the labeler indicates was the start of its marketing of the drug product.

This is the date when the listing record will expire if not updated or certified by the product labeler. The complete list of codes and translations can be found at www. The product’s dosage form is tablet, film coated and is administered via oral form.

The non-proprietary name is sometimes called the generic name.