Ceftriaxone Sodium
- Product NDC
- 82804-066
- 11-digit product format
- 828040066
- Labeler code
- 82804
- Product ID
- 82804-066_790279d4-2456-4091-abec-960b78885432
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Proficient Rx LP
- Application
- ANDA203702
- Marketing category
- ANDA
- Marketing start
- 2017-06-30
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 023Z5BR09K | CEFTRIAXONE SODIUM | 104376-79-6 | CEFTRIAXONE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-066-01 | 82804006601 | 1 VIAL, SINGLE-USE in 1 CARTON (82804-066-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2024-02-02 | No | No | Historical |
| 82804-066-10 | 82804006610 | 10 VIAL, SINGLE-USE in 1 CARTON (82804-066-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2024-02-02 | No | No | Historical |