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Sumadan
Sumadan - 43538-191-16 - (sulfacetamide sodium and sulfur)
Drug Information of Sumadan
| Product NDC: | 43538-191 |
| Proprietary Name: | Sumadan |
| Non Proprietary Name: | sulfacetamide sodium and sulfur |
| Active Ingredient(s): | & nbsp; sulfacetamide sodium and sulfur |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumadan
| Product NDC: | 43538-191 |
| Labeler Name: | Medimetriks Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110801 |
Package Information of Sumadan
| Package NDC: | 43538-191-16 |
| Package Description: | 1 KIT in 1 CARTON (43538-191-16) * 1 BOTTLE, PUMP in 1 CARTON > 454 g in 1 BOTTLE, PUMP * 1 BOTTLE, PUMP in 1 CARTON > 454 g in 1 BOTTLE, PUMP |
NDC Information of Sumadan
| NDC Code | 43538-191-16 |
| Proprietary Name | Sumadan |
| Package Description | 1 KIT in 1 CARTON (43538-191-16) * 1 BOTTLE, PUMP in 1 CARTON > 454 g in 1 BOTTLE, PUMP * 1 BOTTLE, PUMP in 1 CARTON > 454 g in 1 BOTTLE, PUMP |
| Product NDC | 43538-191 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium and sulfur |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Medimetriks Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
