Ceftriaxone Sodium
- Product NDC
- 0781-3206
- 11-digit product format
- 007813206
- Labeler code
- 0781
- Product ID
- 0781-3206_371d8db2-5d67-4339-92b7-aee2a52b2293
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA065169
- Marketing category
- ANDA
- Marketing start
- 2005-05-09
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 250 mg/1
- 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
- Ceftriaxone Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFTRIAXONE SODIUM | 250 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 |
|---|
| 0781-3206-85 | Ceftriaxone Sodium | 1 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 1 | | 24 |
| 0781-3206-85 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 24 |
| 0781-3206-95 | Ceftriaxone Sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 24 |
| 0781-3206-95 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-3206 | CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [SANDOZ INC] | 23 | Current NDC, Legacy NDC, 4 package rows | 20250416_de028434-46cf-44f6-8ac6-889c7c6943b3.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 |
|---|
| 0781-3206-85 | 00781320685 | 1 VIAL, SINGLE-USE in 1 CARTON (0781-3206-85) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2005-05-09 | 0000-00-00 | No | No | Current |
| 0781-3206-95 | 00781320695 | 10 VIAL, SINGLE-USE in 1 CARTON (0781-3206-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2005-05-09 | 0000-00-00 | No | No | Current |