Sepia - 53499-5972-2 - (Sepia)

Alphabetical Index


Drug Information of Sepia

Product NDC: 53499-5972
Proprietary Name: Sepia
Non Proprietary Name: Sepia
Active Ingredient(s): 30    [hp_X]/1 & nbsp;   Sepia
Administration Route(s): SUBLINGUAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sepia

Product NDC: 53499-5972
Labeler Name: Natures Way Holding Co.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060101

Package Information of Sepia

Package NDC: 53499-5972-2
Package Description: 100 TABLET in 1 BOTTLE, GLASS (53499-5972-2)

NDC Information of Sepia

NDC Code 53499-5972-2
Proprietary Name Sepia
Package Description 100 TABLET in 1 BOTTLE, GLASS (53499-5972-2)
Product NDC 53499-5972
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sepia
Dosage Form Name TABLET
Route Name SUBLINGUAL
Start Marketing Date 20060101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natures Way Holding Co.
Substance Name SEPIA OFFICINALIS JUICE
Strength Number 30
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of Sepia


General Information