Ceftriaxone
- Product NDC
- 50090-2628
- 11-digit product format
- 500902628
- Labeler code
- 50090
- Product ID
- 50090-2628_960bc6cb-1809-485b-bab7-f86b9652dd5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA065342
- Marketing category
- ANDA
- Marketing start
- 2008-01-10
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2628-0 | Ceftriaxone | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 10 |
| 50090-2628-0 | Ceftriaxone | 1 in 1 BOX | INJECTION, POWDER, FOR SOLUTION | 1 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2628 | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [A-S MEDICATION SOLUTIONS] | 10 | Legacy NDC, 2 package rows | 20200122_f449e25d-2e52-4a92-9dd5-1e58b3009a9e.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 |
|---|
| 50090-2628-0 | 50090262800 | 1 VIAL in 1 BOX (50090-2628-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2016-11-17 | 0000-00-00 | No | No | Current |