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Sodium Sulfacetamide and Sulfur
Sodium Sulfacetamide and Sulfur - 44523-609-23 - (sodium sulfacetamide, sulfur)
Drug Information of Sodium Sulfacetamide and Sulfur
| Product NDC: | 44523-609 |
| Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Non Proprietary Name: | sodium sulfacetamide, sulfur |
| Active Ingredient(s): | & nbsp; sodium sulfacetamide, sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Sulfacetamide and Sulfur
| Product NDC: | 44523-609 |
| Labeler Name: | BioComp Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110415 |
Package Information of Sodium Sulfacetamide and Sulfur
| Package NDC: | 44523-609-23 |
| Package Description: | 1 KIT in 1 CARTON (44523-609-23) * 454 g in 1 BOTTLE, PLASTIC (44523-605-16) * 473 mL in 1 BOTTLE, PLASTIC |
NDC Information of Sodium Sulfacetamide and Sulfur
| NDC Code | 44523-609-23 |
| Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Package Description | 1 KIT in 1 CARTON (44523-609-23) * 454 g in 1 BOTTLE, PLASTIC (44523-605-16) * 473 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 44523-609 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium sulfacetamide, sulfur |
| Dosage Form Name | KIT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110415 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | BioComp Pharma, Inc. |
| Substance Name | |
| Strength Number | |
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