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NDC 44523-0550-08 Sodium Sulfacetamide, Sulfur 100; 20 mg/g; mg/g Details
Sodium Sulfacetamide, Sulfur 100; 20 mg/g; mg/g
Sodium Sulfacetamide, Sulfur is a TOPICAL EMULSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by BioComp Pharma, Inc.. The primary component is SULFACETAMIDE SODIUM; SULFUR.
Product Information
| NDC | 44523-0550 |
|---|---|
| Product ID | 44523-550_f798f8d7-639f-2a12-e053-6294a90a00fb |
| Associated GPIs | 90059903200918 |
| GCN Sequence Number | 066048 |
| GCN Sequence Number Description | sulfacetamide sodium/sulfur CLEANSER 10 %-2 % TOPICAL |
| HIC3 | Q5S |
| HIC3 Description | TOPICAL SULFONAMIDES |
| GCN | 28226 |
| HICL Sequence Number | 003344 |
| HICL Sequence Number Description | SULFACETAMIDE SODIUM/SULFUR |
| Brand/Generic | Generic |
| Proprietary Name | Sodium Sulfacetamide, Sulfur |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | SULFACETAMIDE SODIUM, SULFUR |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | EMULSION |
| Route | TOPICAL |
| Active Ingredient Strength | 100; 20 |
| Active Ingredient Units | mg/g; mg/g |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Labeler Name | BioComp Pharma, Inc. |
| Pharmaceutical Class | Sulfonamide Antibacterial [EPC], Sulfonamides [CS] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 44523-0550-08 (44523055008)
| NDC Package Code | 44523-550-08 |
|---|---|
| Billing NDC | 44523055008 |
| Package | 227 g in 1 BOTTLE, PLASTIC (44523-550-08) |
| Marketing Start Date | 2011-09-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |