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SEPIA OFFICINALIS - 10191-1569-2 - (CUTTLEFISH)

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Drug Information of SEPIA OFFICINALIS

Product NDC: 10191-1569
Proprietary Name: SEPIA OFFICINALIS
Non Proprietary Name: CUTTLEFISH
Active Ingredient(s): 6    [hp_C]/1 & nbsp;   CUTTLEFISH
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of SEPIA OFFICINALIS

Product NDC: 10191-1569
Labeler Name: Remedy Makers
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20030507

Package Information of SEPIA OFFICINALIS

Package NDC: 10191-1569-2
Package Description: 162 PELLET in 1 VIAL, GLASS (10191-1569-2)

NDC Information of SEPIA OFFICINALIS

NDC Code 10191-1569-2
Proprietary Name SEPIA OFFICINALIS
Package Description 162 PELLET in 1 VIAL, GLASS (10191-1569-2)
Product NDC 10191-1569
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CUTTLEFISH
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20030507
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Remedy Makers
Substance Name CUTTLEFISH
Strength Number 6
Strength Unit [hp_C]/1
Pharmaceutical Classes

Complete Information of SEPIA OFFICINALIS


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