NDC 69152-0055 Lipen 40 (number 55)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69152 - Paramesh Banerji Life Sciences Llc
- 69152-0055 - Lipen 40 (number 55)
Product Characteristics
Product Packages
NDC Code 69152-0055-1
Package Description: 96 PELLET in 1 BOTTLE
Product Details
What is NDC 69152-0055?
What are the uses for Lipen 40 (number 55)?
Which are Lipen 40 (number 55) UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
Which are Lipen 40 (number 55) Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SUCROSE (UNII: C151H8M554)
- LACTOSE (UNII: J2B2A4N98G)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".