Ceftriaxone Sodium
- Product NDC
- 68071-4682
- 11-digit product format
- 680714682
- Labeler code
- 68071
- Product ID
- 68071-4682_bb8ba8d6-e3ea-256f-e053-2a95a90adad8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065169
- Marketing category
- ANDA
- Marketing start
- 2005-05-09
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4682-1 | 68071468201 | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (68071-4682-1) | 2018-12-26 | 0000-00-00 | No | No | Current |