NDC 72275-714 Microvix Lp

Lidocaine, Prilocaine, Benzalkonium Chloride

NDC Product Code 72275-714

NDC 72275-714-77

Package Description: 1 KIT in 1 CARTON * 50 mL in 1 BOTTLE, PUMP (72513-100-01) * 30 g in 1 TUBE (52565-007-30)

NDC Product Information

Microvix Lp with NDC 72275-714 is a a human prescription drug product labeled by Primary Pharmaceuticals, Inc.. The generic name of Microvix Lp is lidocaine, prilocaine, benzalkonium chloride. The product's dosage form is kit and is administered via topical form.

Labeler Name: Primary Pharmaceuticals, Inc.

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Prescription Drug 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.

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Primary Pharmaceuticals, Inc.
Labeler Code: 72275
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. 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. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-20-2019 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: 12-31-2020 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: N 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’.

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