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Colocynthis Homaccord
Colocynthis Homaccord - 50114-7065-1 - (PSEUDOGNAPHALIUM OBTUSIFOLIUM and CITRULLUS COLOCYNTHIS FRUIT PULP and)
Drug Information of Colocynthis Homaccord
| Product NDC: | 50114-7065 |
| Proprietary Name: | Colocynthis Homaccord |
| Non Proprietary Name: | PSEUDOGNAPHALIUM OBTUSIFOLIUM and CITRULLUS COLOCYNTHIS FRUIT PULP and |
| Active Ingredient(s): | 4; 3 [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp; PSEUDOGNAPHALIUM OBTUSIFOLIUM and CITRULLUS COLOCYNTHIS FRUIT PULP and |
| Administration Route(s): | INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Colocynthis Homaccord
| Product NDC: | 50114-7065 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120511 |
Package Information of Colocynthis Homaccord
| Package NDC: | 50114-7065-1 |
| Package Description: | 10 AMPULE in 1 CARTON (50114-7065-1) > 1.1 mL in 1 AMPULE |
NDC Information of Colocynthis Homaccord
| NDC Code | 50114-7065-1 |
| Proprietary Name | Colocynthis Homaccord |
| Package Description | 10 AMPULE in 1 CARTON (50114-7065-1) > 1.1 mL in 1 AMPULE |
| Product NDC | 50114-7065 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PSEUDOGNAPHALIUM OBTUSIFOLIUM and CITRULLUS COLOCYNTHIS FRUIT PULP and |
| Dosage Form Name | INJECTION |
| Route Name | INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20120511 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | CITRULLUS COLOCYNTHIS FRUIT PULP; PSEUDOGNAPHALIUM OBTUSIFOLIUM |
| Strength Number | 4; 3 |
| Strength Unit | [hp_X]/1.1mL; [hp_X]/1.1mL |
| Pharmaceutical Classes |
