NDC 0095-0201 Vosol Hc
NDC Product Code 0095-0201
Proprietary Name: Vosol Hc 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.
NDC Code Structure
- 0095 - Ecr Pharmaceuticals Co., Inc.
- 0095-0201 - Vosol Hc
NDC 0095-0201-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON > 10 mL in 1 BOTTLE, DROPPER
NDC Product Information
Vosol Hc with NDC 0095-0201 is a product labeled by Ecr Pharmaceuticals Co., Inc.. The generic name of Vosol Hc is . The product's dosage form is and is administered via form.
Labeler Name: Ecr Pharmaceuticals Co., Inc.
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.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Ecr Pharmaceuticals Co., Inc.
Labeler Code: 0095
Start Marketing Date: 06-22-2009 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: I 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.
