Home
>
National Drug Code (NDC)
>
Birch Juniper Rejuvenation
Birch Juniper Rejuvenation - 48951-2071-9 - (BETULA PENDULA LEAF JUNIPERUS COMMUNIS FRUIT)
Drug Information of Birch Juniper Rejuvenation
| Product NDC: | 48951-2071 |
| Proprietary Name: | Birch Juniper Rejuvenation |
| Non Proprietary Name: | BETULA PENDULA LEAF JUNIPERUS COMMUNIS FRUIT |
| Active Ingredient(s): | 1; 1 [hp_X]/1; [hp_X]/1 & nbsp; BETULA PENDULA LEAF JUNIPERUS COMMUNIS FRUIT |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Birch Juniper Rejuvenation
| Product NDC: | 48951-2071 |
| Labeler Name: | Uriel Pharmacy Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090901 |
Package Information of Birch Juniper Rejuvenation
| Package NDC: | 48951-2071-9 |
| Package Description: | 5200 SYRUP in 1 BOTTLE, GLASS (48951-2071-9) |
NDC Information of Birch Juniper Rejuvenation
| NDC Code | 48951-2071-9 |
| Proprietary Name | Birch Juniper Rejuvenation |
| Package Description | 5200 SYRUP in 1 BOTTLE, GLASS (48951-2071-9) |
| Product NDC | 48951-2071 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BETULA PENDULA LEAF JUNIPERUS COMMUNIS FRUIT |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Uriel Pharmacy Inc |
| Substance Name | BETULA PENDULA LEAF; JUNIPERUS COMMUNIS FRUIT |
| Strength Number | 1; 1 |
| Strength Unit | [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
