Sulfasalazine
- Product NDC
- 70518-0185
- 11-digit product format
- 705180185
- Labeler code
- 70518
- Product ID
- 70518-0185_e6feff0a-3349-194d-e053-2a95a90acd20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulfasalazine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085828
- Marketing category
- ANDA
- Marketing start
- 2017-01-30
- 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 |
|---|
| 70518-0185-0 | 70518018500 | 30 TABLET in 1 BLISTER PACK (70518-0185-0) | 30 tablet | 2017-01-30 | 0000-00-00 | No | No | Current |