Ceftriaxone Sodium
- Product NDC
- 0409-7338
- 11-digit product format
- 004097338
- Labeler code
- 0409
- Product ID
- 0409-7338_c4d53472-41a6-428e-8935-f2c611729457
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, Inc
- Application
- ANDA065169
- Marketing category
- ANDA
- Marketing start
- 2005-05-09
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ceftriaxone Sodium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFTRIAXONE SODIUM | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 023Z5BR09K |
| Rxcui | 309092, 1665005, 1665021, 1665046 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0409-7338-01 | Ceftriaxone Sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 21 |
| 0409-7338-11 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 21 |
| 0409-7338-20 | Ceftriaxone Sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 5 |
| 0409-7338-21 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0409-7338 | CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] | 20 | Current NDC, Legacy NDC, 2 package rows | 20240113_03283208-8616-4117-9d2b-aa8046017a4f.zip |
| 0409-7338 | CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240113_19141ccd-e66c-49a2-a794-0616028495a7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-7338-01 | 00409733801 | 10 VIAL, SINGLE-USE in 1 CARTON (0409-7338-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7338-11) | 2005-05-09 | 0000-00-00 | No | No | Current |
| 0409-7338-11 | 00409733811 | 1 in 1 VIAL, SINGLE-USE | | | | | Historical |
| 0409-7338-20 | 00409733820 | 10 VIAL, SINGLE-USE in 1 CARTON (0409-7338-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7338-21) | 2018-03-19 | 0000-00-00 | No | No | Current |
| 0409-7338-21 | 00409733821 | 1 in 1 VIAL, SINGLE-USE | | | | | Historical |