CEFDINIR
- Product NDC
- 72189-043
- 11-digit product format
- 721890043
- Labeler code
- 72189
- Product ID
- 72189-043_2c4ea169-07c6-6bde-e063-6394a90a0890
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFDINIR
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065259
- Marketing category
- ANDA
- Marketing start
- 2019-11-25
- 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 |
|---|
| 72189-043-32 | CEFDINIR | 5 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 5 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-043 | CEFDINIR POWDER, FOR SUSPENSION [DIRECT RX] | 8 | Current NDC, Legacy NDC, 1 package rows | 20250123_982d0f53-20bc-1cb4-e053-2995a90ad33c.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 |
|---|
| 72189-043-32 | 72189004332 | 5 mL in 1 BOTTLE (72189-043-32) | 5 ml | 2019-11-25 | 0000-00-00 | No | No | Current |