Ceftriaxone Sodium
- Product NDC
- 50090-4978
- 11-digit product format
- 500904978
- Labeler code
- 50090
- Product ID
- 50090-4978_9ec4aee1-f85a-4b99-8ed4-f48a3023b304
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA203702
- Marketing category
- ANDA
- Marketing start
- 2017-06-30
- 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 |
|---|
| 50090-4978-0 | Ceftriaxone Sodium | 1 in 1 VIAL, SINGLE-USE | INJECTION, POWDER, FOR SOLUTION | 1 | | 3 |
| 50090-4978-0 | Ceftriaxone Sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4978 | CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20200530_cd8c0719-fa52-430d-a9f4-7b326de7a0ae.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 |
|---|
| 50090-4978-0 | 50090497800 | 10 VIAL, SINGLE-USE in 1 CARTON (50090-4978-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2020-03-30 | 0000-00-00 | No | No | Current |