Home
>
National Drug Code (NDC)
>
Androbalance
Androbalance - 57520-0023-1 - (Androstenedione, Dehydroepiandrosterone, Pregenolone, Progesterone, Testosterone)
Drug Information of Androbalance
| Product NDC: | 57520-0023 |
| Proprietary Name: | Androbalance |
| Non Proprietary Name: | Androstenedione, Dehydroepiandrosterone, Pregenolone, 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, Pregenolone, Progesterone, Testosterone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Androbalance
| Product NDC: | 57520-0023 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100201 |
Package Information of Androbalance
| Package NDC: | 57520-0023-1 |
| Package Description: | 30 mL in 1 BOTTLE, SPRAY (57520-0023-1) |
NDC Information of Androbalance
| NDC Code | 57520-0023-1 |
| Proprietary Name | Androbalance |
| Package Description | 30 mL in 1 BOTTLE, SPRAY (57520-0023-1) |
| Product NDC | 57520-0023 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Androstenedione, Dehydroepiandrosterone, Pregenolone, Progesterone, Testosterone |
| Dosage Form Name | SPRAY |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ANDROSTENEDIONE; PRASTERONE; 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 |
