Engystol - 50114-7015-2 - (CYNANCHUM VINCETOXICUM ROOT and SULFUR)

Alphabetical Index


Drug Information of Engystol

Product NDC: 50114-7015
Proprietary Name: Engystol
Non Proprietary Name: CYNANCHUM VINCETOXICUM ROOT and SULFUR
Active Ingredient(s): 6; 4    [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp;   CYNANCHUM VINCETOXICUM ROOT and SULFUR
Administration Route(s): INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Engystol

Product NDC: 50114-7015
Labeler Name: Heel Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110706

Package Information of Engystol

Package NDC: 50114-7015-2
Package Description: 1 AMPULE in 1 CARTON (50114-7015-2) > 1.1 mL in 1 AMPULE

NDC Information of Engystol

NDC Code 50114-7015-2
Proprietary Name Engystol
Package Description 1 AMPULE in 1 CARTON (50114-7015-2) > 1.1 mL in 1 AMPULE
Product NDC 50114-7015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CYNANCHUM VINCETOXICUM ROOT and SULFUR
Dosage Form Name INJECTION
Route Name INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20110706
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name CYNANCHUM VINCETOXICUM ROOT; SULFUR
Strength Number 6; 4
Strength Unit [hp_X]/1.1mL; [hp_X]/1.1mL
Pharmaceutical Classes

Complete Information of Engystol


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