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Acunol
Acunol - 61480-137-05 - (Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur)
Drug Information of Acunol
| Product NDC: | 61480-137 |
| Proprietary Name: | Acunol |
| Non Proprietary Name: | Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur |
| Active Ingredient(s): | 1; 1; 1; 1; 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acunol
| Product NDC: | 61480-137 |
| Labeler Name: | Plymouth Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20060418 |
Package Information of Acunol
| Package NDC: | 61480-137-05 |
| Package Description: | 90 TABLET in 1 BOTTLE (61480-137-05) |
NDC Information of Acunol
| NDC Code | 61480-137-05 |
| Proprietary Name | Acunol |
| Package Description | 90 TABLET in 1 BOTTLE (61480-137-05) |
| Product NDC | 61480-137 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nickel Sulfate, Potassium Bromide, Sodium Bromide, Zinc Sulfate Anhydrous, and Sulfur |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060418 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Plymouth Pharmaceuticals Inc |
| Substance Name | NICKEL SULFATE; POTASSIUM BROMIDE; SODIUM BROMIDE; SULFUR; ZINC SULFATE ANHYDROUS |
| Strength Number | 1; 1; 1; 1; 1 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [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] |
