ceftriaxone
- Product NDC
- 25021-105
- 11-digit product format
- 250210105
- Labeler code
- 25021
- Product ID
- 25021-105_283f5a26-664b-4645-a203-20dc88b4b8df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA065329
- Marketing category
- ANDA
- Marketing start
- 2009-11-05
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 25021-105-10 | ceftriaxone | 25 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 25 | | 19 |
| 25021-105-10 | ceftriaxone | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 19 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 25021-105 | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 19 | Legacy NDC, 2 package rows | 20231115_5cf93bc5-9e4c-4734-bc02-c7d0ac071022.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 |
|---|
| 25021-105-10 | 25021010510 | 25 VIAL in 1 CARTON (25021-105-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 25 vial | 2009-11-05 | 0000-00-00 | No | No | Current |
| 25021-105-66 | 25021010566 | 25 VIAL in 1 CARTON (25021-105-66) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 25 vial | 2015-07-01 | 0000-00-00 | No | No | Current |