SUPRAX
- Product NDC
- 27437-201
- 11-digit product format
- 274370201
- Labeler code
- 27437
- Product ID
- 27437-201_0e44b51b-cba9-4dc5-8ee1-2d151ad24def
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA065130
- Marketing category
- ANDA
- Marketing start
- 2008-04-01
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 400 mg/1
- 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 |
|---|
| 27437-201-01 | 27437020101 | 100 TABLET in 1 BOTTLE (27437-201-01) | 100 tablet | 2008-04-01 | 0000-00-00 | No | No | Current |
| 27437-201-08 | 27437020108 | 50 TABLET in 1 BOTTLE (27437-201-08) | 50 tablet | 2008-04-01 | 0000-00-00 | No | No | Current |
| 27437-201-10 | 27437020110 | 10 TABLET in 1 BOTTLE (27437-201-10) | 10 tablet | 2008-04-01 | 0000-00-00 | No | No | Current |
| 27437-201-25 | 27437020125 | 1 BOTTLE in 1 CARTON (27437-201-25) > 2 TABLET in 1 BOTTLE | 1 bottle | 2008-04-01 | 0000-00-00 | No | No | Current |