CEFTRIAXONE
- Product NDC
- 42254-152
- 11-digit product format
- 422540152
- Labeler code
- 42254
- Product ID
- 42254-152_1781fc07-5a2a-4b31-aad9-d0457eb704f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFTRIAXONE
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Rebel Distributors Corp
- Application
- ANDA065391
- Marketing category
- ANDA
- Marketing start
- 2007-04-12
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 42254-152-10 | CEFTRIAXONE | 1 in 1 BOX | INJECTION, POWDER, FOR SOLUTION | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42254-152 | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20120420_1781fc07-5a2a-4b31-aad9-d0457eb704f4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42254-152-10 | 42254015210 | 1 in 1 BOX | Historical |