cefuroxime axetil
- Product NDC
- 68180-302
- 11-digit product format
- 681800302
- Labeler code
- 68180
- Product ID
- 68180-302_6def7bcd-63fa-47aa-88dd-f7073d3d1fc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefuroxime axetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA065135
- Marketing category
- ANDA
- Marketing start
- 2008-10-08
- Marketing end
- 0000-00-00
- Substance
- CEFUROXIME AXETIL
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68180-302-20 | 68180030220 | 20 TABLET in 1 BOTTLE (68180-302-20) | 20 tablet | 2008-10-08 | 0000-00-00 | No | No | Current |
| 68180-302-60 | 68180030260 | 60 TABLET in 1 BOTTLE (68180-302-60) | 60 tablet | 2008-10-08 | 0000-00-00 | No | No | Current |