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