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SSD - 49884-600-36 - (silver sulfadiazine)
Drug Information of SSD
| Product NDC: | 49884-600 |
| Proprietary Name: | SSD |
| Non Proprietary Name: | silver sulfadiazine |
| Active Ingredient(s): | 10 g/1000g & nbsp; silver sulfadiazine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SSD
| Product NDC: | 49884-600 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018578 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970918 |
Package Information of SSD
| Package NDC: | 49884-600-36 |
| Package Description: | 50 g in 1 JAR (49884-600-36) |
NDC Information of SSD
| NDC Code | 49884-600-36 |
| Proprietary Name | SSD |
| Package Description | 50 g in 1 JAR (49884-600-36) |
| Product NDC | 49884-600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | silver sulfadiazine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19970918 |
| Marketing Category Name | NDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | SILVER SULFADIAZINE |
| Strength Number | 10 |
| Strength Unit | g/1000g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
