Cefdinir
- Product NDC
- 76420-328
- 11-digit product format
- 764200328
- Labeler code
- 76420
- Product ID
- 76420-328_331b63bf-fd36-155d-e063-6294a90aec23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA065259
- Marketing category
- ANDA
- Marketing start
- 2007-05-07
- 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 | 309054, 476576 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76420-328-01 | Cefdinir | 100 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 100 | | 1 |
| 76420-328-60 | Cefdinir | 60 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-328 | CEFDINIR POWDER, FOR SUSPENSION [ASCLEMED USA, INC.] | 1 | Current NDC, 2 package rows | 20250424_e90660c8-2714-4592-aeaa-bc9ceb26057c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-328-01 | 76420032801 | 100 mL in 1 BOTTLE (76420-328-01) | 100 ml | 2025-04-19 | No | No | Historical |
| 76420-328-60 | 76420032860 | 60 mL in 1 BOTTLE (76420-328-60) | 60 ml | 2025-04-19 | No | No | Historical |