CEFTRIAXONE
- Product NDC
- 64679-703
- 11-digit product format
- 646790703
- Labeler code
- 64679
- Product ID
- 64679-703_ff8335d4-aa03-4918-8f84-71ae42c92630
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFTRIAXONE
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA065391
- Marketing category
- ANDA
- Marketing start
- 2007-04-12
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 2 g/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
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CEFTRIAXONE SODIUM | ACTIVE INGREDIENT | 023Z5BR09K | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [WOCKHARDT USA LLC.] | 3 | |
| CEFTRIAXONE | ACTIVE MOIETY | 75J73V1629 | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [WOCKHARDT USA LLC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64679-703 | CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [WOCKHARDT USA LLC.] | 8 | Legacy NDC | 20201218_dc28e719-6fe0-4d9e-a624-adb76b04b299.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64679-703-01 | 64679070301 | 10 INJECTION, POWDER, FOR SOLUTION in 1 BOX (64679-703-01) | 2007-04-12 | 0000-00-00 | No | No | Current |
| 64679-703-02 | 64679070302 | 1 INJECTION, POWDER, FOR SOLUTION in 1 BOX (64679-703-02) | 2007-04-12 | 0000-00-00 | No | No | Current |