Cefpodoxime Proxetil
- Product NDC
- 68071-3616
- 11-digit product format
- 680713616
- Labeler code
- 68071
- Product ID
- 68071-3616_1b40454e-994c-39d8-e063-6394a90a97cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefpodoxime Proxetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210568
- Marketing category
- ANDA
- Marketing start
- 2023-03-01
- Substance
- CEFPODOXIME PROXETIL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2TB00A1Z7N | CEFPODOXIME PROXETIL | 87239-81-4 | CEFPODOXIME PROXETIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3616-4 | 68071361604 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-3616-4) | 2024-06-19 | No | No | Historical |