Proprietary Name: Cisatracurium Besylate 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. Non-Proprietary Name: What is the Non-Proprietary Name?The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Package Description: 10 VIAL in 1 CARTON > 10 mL in 1 VIAL
Cisatracurium Besylate with NDC 25021-670 is a product labeled by Sagent Pharmaceuticals. The generic name of Cisatracurium Besylate is . The product's dosage form is and is administered via form.
Labeler Name: Sagent Pharmaceuticals
Dosage Form: - Product Type: What kind of product is this?Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Labeler Name: Sagent Pharmaceuticals Labeler Code: 25021 Start Marketing Date: 12-01-2019 What is the Start Marketing Date?This is the date that the labeler indicates was the start of its marketing of the drug product. Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?This is the date when the listing record will expire if not updated or certified by the product labeler. Exclude Flag: E What is the NDC Exclude Flag?This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Previous Code: 25021-669
Next Code: 25021-671