cefdinir
- Product NDC
- 50090-5811
- 11-digit product format
- 500905811
- Labeler code
- 50090
- Product ID
- 50090-5811_af5bca73-a913-4d8f-954d-a6ed48e02d5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210534
- Marketing category
- ANDA
- Marketing start
- 2021-02-20
- 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 |
|---|
| 50090-5811-0 | cefdinir | 60 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 60 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5811 | CEFDINIR POWDER, FOR SUSPENSION [A-S MEDICATION SOLUTIONS] | 7 | Current NDC, Legacy NDC, 1 package rows | 20231125_7bbcc4ac-c964-4c6b-88c0-11c0ba9933db.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 |
|---|
| 50090-5811-0 | 50090581100 | 60 mL in 1 BOTTLE (50090-5811-0) | 60 ml | 2021-10-18 | 0000-00-00 | No | No | Current |