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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cefpodoxime Proxetil
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFPODOXIME PROXETIL | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2TB00A1Z7N |
| Rxcui | 309076 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3616-4 | Cefpodoxime Proxetil | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3616 | CEFPODOXIME PROXETIL TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Current NDC, 1 package rows | 20240620_1b405104-650b-c8e3-e063-6294a90a9e8a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |