Ceftriaxone
- Product NDC
- 50090-0943
- 11-digit product format
- 500900943
- Labeler code
- 50090
- Product ID
- 50090-0943_f1215b9a-a4be-408f-af20-bccc5de0c718
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA065230
- Marketing category
- ANDA
- Marketing start
- 2005-08-02
- 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
- 2019-12-31
- 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 |
|---|
| 50090-0943-0 | Ceftriaxone | 1 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 1 | | 3 |
| 50090-0943-0 | Ceftriaxone | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0943 | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20171117_467f49f7-1a35-49c1-88aa-acc2f27adc2b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-0943-0 | 50090094300 | 1 in 1 CARTON | Historical |