Home
>
National Drug Code (NDC)
>
Osteodoron AM Bone Support
Osteodoron AM Bone Support - 48951-7096-4 - (PUMPKIN SILICON DIOXIDE CALCIUM FLUORIDE FLUORAPATITE)
Drug Information of Osteodoron AM Bone Support
| Product NDC: | 48951-7096 |
| Proprietary Name: | Osteodoron AM Bone Support |
| Non Proprietary Name: | PUMPKIN SILICON DIOXIDE CALCIUM FLUORIDE FLUORAPATITE |
| Active Ingredient(s): | 6; 6; 3; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; PUMPKIN SILICON DIOXIDE CALCIUM FLUORIDE FLUORAPATITE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Osteodoron AM Bone Support
| Product NDC: | 48951-7096 |
| Labeler Name: | Uriel Pharmacy Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090901 |
Package Information of Osteodoron AM Bone Support
| Package NDC: | 48951-7096-4 |
| Package Description: | 1 POWDER in 1 BOTTLE, GLASS (48951-7096-4) |
NDC Information of Osteodoron AM Bone Support
| NDC Code | 48951-7096-4 |
| Proprietary Name | Osteodoron AM Bone Support |
| Package Description | 1 POWDER in 1 BOTTLE, GLASS (48951-7096-4) |
| Product NDC | 48951-7096 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PUMPKIN SILICON DIOXIDE CALCIUM FLUORIDE FLUORAPATITE |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Uriel Pharmacy Inc |
| Substance Name | CALCIUM FLUORIDE; FLUORAPATITE; PUMPKIN; SILICON DIOXIDE |
| Strength Number | 6; 6; 3; 6 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
