Product NDC: | 0093-9614 |
Proprietary Name: | Silver Nitrate |
Non Proprietary Name: | Silver Nitrate |
Active Ingredient(s): | .005 g/mL & nbsp; Silver Nitrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0093-9614 |
Labeler Name: | Teva Pharmaceuticals USA Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19910101 |
Package NDC: | 0093-9614-13 |
Package Description: | 960 mL in 1 BOTTLE (0093-9614-13) |
NDC Code | 0093-9614-13 |
Proprietary Name | Silver Nitrate |
Package Description | 960 mL in 1 BOTTLE (0093-9614-13) |
Product NDC | 0093-9614 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Silver Nitrate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19910101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Teva Pharmaceuticals USA Inc |
Substance Name | SILVER NITRATE |
Strength Number | .005 |
Strength Unit | g/mL |
Pharmaceutical Classes |