Sulfasalazine
- Product NDC
- 0591-0796
- 11-digit product format
- 005910796
- Labeler code
- 0591
- Product ID
- 0591-0796_9174d15c-8a8b-4a9b-9ef2-f38b25a3ccb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulfasalazine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA085828
- Marketing category
- ANDA
- Marketing start
- 1982-10-01
- Marketing end
- 0000-00-00
- Substance
- SULFASALAZINE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Aminosalicylate [EPC], Aminosalicylic Acids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-0796-01 | 00591079601 | 100 TABLET in 1 BOTTLE, PLASTIC (0591-0796-01) | 100 tablet | 1982-10-01 | 0000-00-00 | No | No | Current |
| 0591-0796-05 | 00591079605 | 500 TABLET in 1 BOTTLE, PLASTIC (0591-0796-05) | 500 tablet | 1982-10-01 | 0000-00-00 | No | No | Current |
| 0591-0796-10 | 00591079610 | 1000 TABLET in 1 BOTTLE, PLASTIC (0591-0796-10) | 1000 tablet | 1982-10-01 | 0000-00-00 | No | No | Current |