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Androbalance
Androbalance - 43857-0102-1 - (Androstenedione, Dehydroepiandrosterone, Pregnenolone, Progesterone, Testosterone)
Drug Information of Androbalance
| Product NDC: | 43857-0102 |
| Proprietary Name: | Androbalance |
| Non Proprietary Name: | Androstenedione, Dehydroepiandrosterone, Pregnenolone, Progesterone, Testosterone |
| Active Ingredient(s): | 6; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Androstenedione, Dehydroepiandrosterone, Pregnenolone, Progesterone, Testosterone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Androbalance
| Product NDC: | 43857-0102 |
| Labeler Name: | BioActive Nutritional, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20121026 |
Package Information of Androbalance
| Package NDC: | 43857-0102-1 |
| Package Description: | 30 mL in 1 BOTTLE, SPRAY (43857-0102-1) |
NDC Information of Androbalance
| NDC Code | 43857-0102-1 |
| Proprietary Name | Androbalance |
| Package Description | 30 mL in 1 BOTTLE, SPRAY (43857-0102-1) |
| Product NDC | 43857-0102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Androstenedione, Dehydroepiandrosterone, Pregnenolone, Progesterone, Testosterone |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121026 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | BioActive Nutritional, Inc. |
| Substance Name | 7-OXO-PRASTERONE; ANDROSTENEDIONE; PREGNENOLONE; PROGESTERONE; TESTOSTERONE |
| Strength Number | 6; 6; 8; 8; 8 |
| Strength Unit | [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] |
