NDC 61480-127
Eczemol
Potassium Bromide, Nickel Sulfate, And Sulfur
Eczemol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Plymouth Healthcare Products Llc. The primary component is Potassium Bromide; Nickel Sulfate; Sulfur.
| Product ID | 61480-127_b8e515bd-8ee5-1715-e053-2995a90a5d2d |
| NDC | 61480-127 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Eczemol |
| Generic Name | Potassium Bromide, Nickel Sulfate, And Sulfur |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2001-11-15 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | PLYMOUTH HEALTHCARE PRODUCTS LLC |
| Substance Name | POTASSIUM BROMIDE; NICKEL SULFATE; SULFUR |
| Active Ingredient Strength | 1 [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
Packaging
NDC 61480-127-05
100 TABLET in 1 BOTTLE (61480-127-05)
| Marketing Start Date | 2001-11-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 61480-127-05 [61480012705]
Eczemol TABLET
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-11-15 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| POTASSIUM BROMIDE | 1 [hp_X]/1 |
OpenFDA Data
| SPL SET ID: | 981e9f3d-b608-4a5e-92f8-895b22da12f4 |
| Manufacturer | |
| UNII |
Trademark Results [Eczemol]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ECZEMOL 78647330 3093206 Live/Registered |
INNOVA BIOTECH LLC 2005-06-09 |
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