Sulfacetamide Sodium
- Product NDC
- 17478-221
- 11-digit product format
- 174780221
- Labeler code
- 17478
- Product ID
- 17478-221_074add77-38d0-4952-a044-9366a5197fc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulfacetamide Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- ANDA040215
- Marketing category
- ANDA
- Marketing start
- 2014-09-11
- Marketing end
- 0000-00-00
- Substance
- SULFACETAMIDE SODIUM
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-221-12 | 17478022112 | 1 BOTTLE, DROPPER in 1 CARTON (17478-221-12) > 15 mL in 1 BOTTLE, DROPPER | 2014-09-11 | 0000-00-00 | No | No | Current |