DNA - 57520-0740-1 - (DNA,)

Alphabetical Index


Drug Information of DNA

Product NDC: 57520-0740
Proprietary Name: DNA
Non Proprietary Name: DNA,
Active Ingredient(s): 12    [hp_X]/mL & nbsp;   DNA,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of DNA

Product NDC: 57520-0740
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110801

Package Information of DNA

Package NDC: 57520-0740-1
Package Description: 60 mL in 1 BOTTLE, DROPPER (57520-0740-1)

NDC Information of DNA

NDC Code 57520-0740-1
Proprietary Name DNA
Package Description 60 mL in 1 BOTTLE, DROPPER (57520-0740-1)
Product NDC 57520-0740
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DNA,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name HERRING SPERM DNA
Strength Number 12
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of DNA


General Information