36987-1492 NDC - WHITE POTATO ()

Drug Information

Product NDC: 36987-1492

Proprietary Name: White Potato

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	36987-1492-1	5 mL in 1 VIAL, MULTI-DOSE (36987-1492-1)
2	36987-1492-2	10 mL in 1 VIAL, MULTI-DOSE (36987-1492-2)
3	36987-1492-3	30 mL in 1 VIAL, MULTI-DOSE (36987-1492-3)
4	36987-1492-4	50 mL in 1 VIAL, MULTI-DOSE (36987-1492-4)

Field Name	Field Value	Definition
PRODUCT NDC	36987-1492	The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAME	White Potato	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	8/29/1972	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Nelco Laboratories, Inc.	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.

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This page was last updated on: 2/1/2023