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Psorizide Ultra
Psorizide Ultra - 61480-124-05 - (Potassium Bromide, Nickel Sulfate, and Zinc Bromide)
Drug Information of Psorizide Ultra
| Product NDC: | 61480-124 |
| Proprietary Name: | Psorizide Ultra |
| Non Proprietary Name: | Potassium Bromide, Nickel Sulfate, and Zinc Bromide |
| Active Ingredient(s): | 1; 1; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; Potassium Bromide, Nickel Sulfate, and Zinc Bromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Psorizide Ultra
| Product NDC: | 61480-124 |
| Labeler Name: | Plymouth Pharmaceuticals Inc dba Loma Lux Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19971001 |
Package Information of Psorizide Ultra
| Package NDC: | 61480-124-05 |
| Package Description: | 100 TABLET in 1 BOTTLE (61480-124-05) |
NDC Information of Psorizide Ultra
| NDC Code | 61480-124-05 |
| Proprietary Name | Psorizide Ultra |
| Package Description | 100 TABLET in 1 BOTTLE (61480-124-05) |
| Product NDC | 61480-124 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Bromide, Nickel Sulfate, and Zinc Bromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19971001 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Plymouth Pharmaceuticals Inc dba Loma Lux Laboratories |
| Substance Name | NICKEL SULFATE; POTASSIUM BROMIDE; ZINC BROMIDE |
| Strength Number | 1; 1; 4 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |
