Cefdinir
- Product NDC
- 50090-2735
- 11-digit product format
- 500902735
- Labeler code
- 50090
- Product ID
- 50090-2735_664df642-b804-4457-b571-d45e9cd547be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065473
- Marketing category
- ANDA
- Marketing start
- 2007-12-14
- Substance
- CEFDINIR
- Active strength
- 250 mg/5mL
- 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
- Cefdinir
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFDINIR | 250 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | CI0FAO63WC |
| Rxcui | 476576 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2735-0 | Cefdinir | 60 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 60 | | 10 |
| 50090-2735-0 | Cefdinir | 1 in 1 CARTON | POWDER, FOR SUSPENSION | 1 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2735 | CEFDINIR POWDER, FOR SUSPENSION [A-S MEDICATION SOLUTIONS] | 10 | Current NDC, Legacy NDC, 2 package rows | 20240229_beeb9480-f9f9-44ae-93f3-6f4da81888f5.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 |
|---|
| 50090-2735-0 | 50090273500 | 1 BOTTLE in 1 CARTON (50090-2735-0) / 60 mL in 1 BOTTLE | 1 bottle | 2016-12-29 | 0000-00-00 | No | No | Current |