69152-0570 NDC - JALPET 40 (NUMBER 570) ()

Drug Information

Field Name	Field Value
Labeler Name:	Paramesh Banerji Life Sciences LLC
Product Type:
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	10/24/2014

No.	Package Code	Package Description	Billing Unit
1	69152-0570-1	96 PELLET in 1 BOTTLE (69152-0570-1)

Field Name	Field Value	Definition
PRODUCT NDC	69152-0570	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PROPRIETARY NAME	Jalpet 40 (Number 570)	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	10/24/2014	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Paramesh Banerji Life Sciences LLC	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.