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Spascupreel
Spascupreel - 52919-141-10 - (ACONITUM NAPELLUS and AMMONIUM BROMIDE and CITRULLUS COLOCYNTHIS FRUIT PULP and ATROPINE SULFATE and GELSEMIUM SEMPERVIRENS ROOT and MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE and VERATRUM ALBUM ROOT and)
Drug Information of Spascupreel
| Product NDC: | 52919-141 |
| Proprietary Name: | Spascupreel |
| Non Proprietary Name: | ACONITUM NAPELLUS and AMMONIUM BROMIDE and CITRULLUS COLOCYNTHIS FRUIT PULP and ATROPINE SULFATE and GELSEMIUM SEMPERVIRENS ROOT and MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE and VERATRUM ALBUM ROOT and |
| Active Ingredient(s): | 6; 4; 4; 6; 3; 4; 6; 6; 6; 2; 6 [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp; ACONITUM NAPELLUS and AMMONIUM BROMIDE and CITRULLUS COLOCYNTHIS FRUIT PULP and ATROPINE SULFATE and GELSEMIUM SEMPERVIRENS ROOT and MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE and VERATRUM ALBUM ROOT and |
| Administration Route(s): | INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Spascupreel
| Product NDC: | 52919-141 |
| Labeler Name: | Hameln Pharma GmbH |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110120 |
Package Information of Spascupreel
| Package NDC: | 52919-141-10 |
| Package Description: | 1.1 mL in 1 AMPULE (52919-141-10) |
NDC Information of Spascupreel
| NDC Code | 52919-141-10 |
| Proprietary Name | Spascupreel |
| Package Description | 1.1 mL in 1 AMPULE (52919-141-10) |
| Product NDC | 52919-141 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ACONITUM NAPELLUS and AMMONIUM BROMIDE and CITRULLUS COLOCYNTHIS FRUIT PULP and ATROPINE SULFATE and GELSEMIUM SEMPERVIRENS ROOT and MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE and VERATRUM ALBUM ROOT and |
| Dosage Form Name | INJECTION |
| Route Name | INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20110120 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Hameln Pharma GmbH |
| Substance Name | ACONITUM NAPELLUS; AMANITA MUSCARIA VAR. MUSCARIA; AMMONIUM BROMIDE; ATROPINE SULFATE; CHAMOMILE; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA FLOWER; VERATRUM ALBUM ROOT |
| Strength Number | 6; 4; 4; 6; 3; 4; 6; 6; 6; 2; 6 |
| Strength Unit | [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL |
| Pharmaceutical Classes |
