| 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 |