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NDC 61480-0124-05 Psorizide Ultra 1; 1; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1 Details
Psorizide Ultra 1; 1; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1
Psorizide Ultra is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PLYMOUTH HEALTHCARE PRODUCTS LLC. The primary component is NICKEL SULFATE; POTASSIUM BROMIDE; ZINC BROMIDE.
Product Information
| NDC | 61480-0124 |
|---|---|
| Product ID | 61480-124_eeb57e23-4659-a6f0-e053-2995a90a3c75 |
| Associated GPIs | 99870010000300 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Psorizide Ultra |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Potassium Bromide, Nickel Sulfate, and Zinc Bromide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 1; 1; 4 |
| Active Ingredient Units | [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Substance Name | NICKEL SULFATE; POTASSIUM BROMIDE; ZINC BROMIDE |
| Labeler Name | PLYMOUTH HEALTHCARE PRODUCTS LLC |
| Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 61480-0124-05 (61480012405)
| NDC Package Code | 61480-124-05 |
|---|---|
| Billing NDC | 61480012405 |
| Package | 100 TABLET in 1 BOTTLE (61480-124-05) |
| Marketing Start Date | 1997-10-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |