Ceftriaxone Sodium
- Product NDC
- 60505-6152
- 11-digit product format
- 605056152
- Labeler code
- 60505
- Product ID
- 60505-6152_0432e6c3-ad77-726c-e063-6294a90a798c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Apotex Corp.
- Application
- ANDA203702
- Marketing category
- ANDA
- Marketing start
- 2017-06-30
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 500 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 | 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 |
|---|
| 60505-6152-1 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 11 |
| 60505-6152-1 | Ceftriaxone Sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 11 |
| 60505-6152-4 | Ceftriaxone Sodium | 1 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 1 | | 11 |
| 60505-6152-4 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-6152 | CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [APOTEX CORP.] | 11 | Current NDC, Legacy NDC, 4 package rows | 20230831_5116231f-82d1-44be-b08e-560c9a50e5c5.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 |
|---|
| 60505-6152-1 | 60505615201 | 10 VIAL, SINGLE-USE in 1 CARTON (60505-6152-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2017-06-30 | 0000-00-00 | No | No | Current |
| 60505-6152-4 | 60505615204 | 1 VIAL, SINGLE-USE in 1 CARTON (60505-6152-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2017-06-30 | 0000-00-00 | No | No | Current |