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Hormone Combination
Hormone Combination - 43742-0161-1 - (Salsolinol hydrochloride, Cholesterinum, Dehydroepiandrsterone, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone aceticum, Aldosterone, Androsterone, Follicle stimulating hormone,)
Drug Information of Hormone Combination
| Product NDC: | 43742-0161 |
| Proprietary Name: | Hormone Combination |
| Non Proprietary Name: | Salsolinol hydrochloride, Cholesterinum, Dehydroepiandrsterone, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone aceticum, Aldosterone, Androsterone, Follicle stimulating hormone, |
| Active Ingredient(s): | 12; 12; 6; 12; 8; 12; 6; 8; 6; 8; 8 [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Salsolinol hydrochloride, Cholesterinum, Dehydroepiandrsterone, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone aceticum, Aldosterone, Androsterone, Follicle stimulating hormone, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hormone Combination
| Product NDC: | 43742-0161 |
| Labeler Name: | Deseret Biologicals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120924 |
Package Information of Hormone Combination
| Package NDC: | 43742-0161-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0161-1) |
NDC Information of Hormone Combination
| NDC Code | 43742-0161-1 |
| Proprietary Name | Hormone Combination |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0161-1) |
| Product NDC | 43742-0161 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Salsolinol hydrochloride, Cholesterinum, Dehydroepiandrsterone, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone aceticum, Aldosterone, Androsterone, Follicle stimulating hormone, |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120924 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Deseret Biologicals, Inc. |
| Substance Name | ALDOSTERONE; ANDROSTERONE; CHOLESTEROL; CORTISONE ACETATE; ESTRONE; FOLLITROPIN; PRASTERONE; PROGESTERONE; SALSOLINOL HYDROCHLORIDE; SUS SCROFA OVARY; TESTOSTERONE |
| Strength Number | 12; 12; 6; 12; 8; 12; 6; 8; 6; 8; 8 |
| Strength Unit | [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC],Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Gonadotropin [EPC],Gonadotropins [Chemical/Ingredient] |
