Ceftriaxone
- Product NDC
- 70518-3355
- 11-digit product format
- 705183355
- Labeler code
- 70518
- Product ID
- 70518-3355_d7c1d243-71cc-5b75-e053-2a95a90a5dbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065342
- Marketing category
- ANDA
- Marketing start
- 2022-02-02
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3355-0 | 70518335500 | 25 VIAL in 1 BOX (70518-3355-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70518-3355-1) | 25 vial | 2022-02-02 | 0000-00-00 | No | No | Current |