SUPRAX
- Product NDC
- 27437-206
- 11-digit product format
- 274370206
- Labeler code
- 27437
- Product ID
- 27437-206_0e44b51b-cba9-4dc5-8ee1-2d151ad24def
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA065355
- Marketing category
- ANDA
- Marketing start
- 2007-06-01
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 200 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 27437-206-01 | 27437020601 | 100 mL in 1 BOTTLE (27437-206-01) | 100 ml | 2007-06-01 | 0000-00-00 | No | No | Current |
| 27437-206-02 | 27437020602 | 75 mL in 1 BOTTLE (27437-206-02) | 75 ml | 2007-06-01 | 0000-00-00 | No | No | Current |
| 27437-206-03 | 27437020603 | 50 mL in 1 BOTTLE (27437-206-03) | 50 ml | 2007-06-01 | 0000-00-00 | No | No | Current |
| 27437-206-04 | 27437020604 | 1 BOTTLE in 1 CARTON (27437-206-04) > 10 mL in 1 BOTTLE | 1 bottle | 2007-06-01 | 0000-00-00 | No | No | Current |
| 27437-206-05 | 27437020605 | 25 mL in 1 BOTTLE (27437-206-05) | 25 ml | 2007-06-01 | 0000-00-00 | No | No | Current |
| 27437-206-06 | 27437020606 | 37.5 mL in 1 BOTTLE (27437-206-06) | 37.5 ml | 2007-06-01 | 0000-00-00 | No | No | Current |