Cefpodoxime Proxetil
- Product NDC
- 69292-510
- 11-digit product format
- 692920510
- Labeler code
- 69292
- Product ID
- 69292-510_849a91fa-6412-4985-a567-528c508e6815
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefpodoxime Proxetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amici Pharmaceuticals, LLC.
- Application
- ANDA210568
- Marketing category
- ANDA
- Marketing start
- 2022-08-26
- Marketing end
- 0000-00-00
- Substance
- CEFPODOXIME PROXETIL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69292-510 | CEFPODOXIME PROXETIL TABLET, FILM COATED [AMICI PHARMACEUTICALS, LLC.] | 1 | Legacy NDC | 20220902_849a91fa-6412-4985-a567-528c508e6815.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69292-510-01 | 69292051001 | 100 TABLET, FILM COATED in 1 BOTTLE (69292-510-01) | 2022-08-26 | 0000-00-00 | No | No | Current |
| 69292-510-50 | 69292051050 | 500 TABLET, FILM COATED in 1 BOTTLE (69292-510-50) | 2022-08-26 | 0000-00-00 | No | No | Current |