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NDC 44523-0602-01 SODIUM SULFACETAMIDE AND SULFUR 100; 50 mg/g; mg/g Details
SODIUM SULFACETAMIDE AND SULFUR 100; 50 mg/g; mg/g
SODIUM SULFACETAMIDE AND SULFUR is a TOPICAL LOTION 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 | 44523-0602 |
|---|---|
| Product ID | 44523-602_f7993689-bf1d-56b7-e053-6394a90af46b |
| Associated GPIs | 90059903204110 |
| GCN Sequence Number | 045334 |
| GCN Sequence Number Description | sulfacetamide sodium/sulfur LOTION 10-5%(W/V) TOPICAL |
| HIC3 | Q5S |
| HIC3 Description | TOPICAL SULFONAMIDES |
| GCN | 15411 |
| HICL Sequence Number | 003344 |
| HICL Sequence Number Description | SULFACETAMIDE SODIUM/SULFUR |
| Brand/Generic | Generic |
| Proprietary Name | SODIUM SULFACETAMIDE AND SULFUR |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | SULFACETAMIDE SODIUM, SULFUR |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | LOTION |
| Route | TOPICAL |
| Active Ingredient Strength | 100; 50 |
| 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 44523-0602-01 (44523060201)
| NDC Package Code | 44523-602-01 |
|---|---|
| Billing NDC | 44523060201 |
| Package | 1 BOTTLE, PLASTIC in 1 CARTON (44523-602-01) / 25 g in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2011-04-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |