Cefdinir
- Product NDC
- 68788-7339
- 11-digit product format
- 687887339
- Labeler code
- 68788
- Product ID
- 68788-7339_5e9ddbe6-73b7-49a4-9291-3c0c2792c1d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065434
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Substance
- CEFDINIR
- Active strength
- 300 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cefdinir
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFDINIR | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | CI0FAO63WC |
| Rxcui | 200346 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-7339-2 | Cefdinir | 20 in 1 BOTTLE | CAPSULE | 20 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7339 | CEFDINIR CAPSULE [PREFERRED PHARMACEUTICALS INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250217_c3892cd7-0e98-4ba3-a845-4aedf6c2a830.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7339-2 | 68788733902 | 20 CAPSULE in 1 BOTTLE (68788-7339-2) | 20 capsule | 2019-03-12 | 0000-00-00 | No | No | Current |