sulfacetamide
- Product NDC
- 60758-018
- 11-digit product format
- 607580018
- Labeler code
- 60758
- Product ID
- 60758-018_3b8e653f-08fa-42f5-bbc1-1890f1103cd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sulfacetamide sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Pacific Pharma, Inc.
- Application
- ANDA080028
- Marketing category
- ANDA
- Marketing start
- 2015-02-06
- 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
- 2020-12-31
- 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 |
|---|
| 60758-018-05 | 60758001805 | 1 BOTTLE, DROPPER in 1 CARTON (60758-018-05) > 5 mL in 1 BOTTLE, DROPPER | 2015-02-06 | 0000-00-00 | No | No | Current |