Sulfasalazine
- Product NDC
- 50268-730
- 11-digit product format
- 502680730
- Labeler code
- 50268
- Product ID
- 50268-730_d5dfc328-99dc-5245-e053-2a95a90a329d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulfasalazine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA085828
- Marketing category
- ANDA
- Marketing start
- 2014-01-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-730-15 | 50268073015 | 50 BLISTER PACK in 1 BOX (50268-730-15) > 1 TABLET in 1 BLISTER PACK (50268-730-11) | 50 blister pack | 2014-01-14 | 0000-00-00 | No | No | Current |