Sodium sulfacetamide
- Product NDC
- 68682-010
- 11-digit product format
- 686820010
- Labeler code
- 68682
- Product ID
- 68682-010_4dcab06b-56fb-4e42-aae0-6e8840ddd80a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium sulfacetamide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA019931
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-12-18
- Substance
- SULFACETAMIDE SODIUM
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium sulfacetamide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFACETAMIDE SODIUM | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4NRT660KJQ |
| Rxcui | 1006688 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68682-010-04 | Sodium sulfacetamide | 1 in 1 CARTON | LOTION | 1 | | 5 |
| 68682-010-04 | Sodium sulfacetamide | 118 mL in 1 BOTTLE, PLASTIC | LOTION | 118 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68682-010 | SODIUM SULFACETAMIDE LOTION [OCEANSIDE PHARMACEUTICALS] | 5 | Current NDC, Legacy NDC, 2 package rows | 20210113_6fa7399b-4ced-492d-b6f6-cf155764087a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68682-010-04 | 68682001004 | 1 BOTTLE, PLASTIC in 1 CARTON (68682-010-04) / 118 mL in 1 BOTTLE, PLASTIC | 2015-12-18 | 0000-00-00 | No | No | Current |