Ceftriaxone
- Product NDC
- 25021-108
- 11-digit product format
- 250210108
- Labeler code
- 25021
- Product ID
- 25021-108_d1c0402f-3fac-449c-88a0-99b510b5397b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA065328
- Marketing category
- ANDA
- Marketing start
- 2009-11-05
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 10 g/100mL
- 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 |
|---|
| 25021-108-69 | 25021010869 | 1 BOTTLE in 1 CARTON (25021-108-69) > 100 mL in 1 BOTTLE | 1 bottle | 2015-07-01 | 0000-00-00 | No | No | Current |
| 25021-108-99 | 25021010899 | 1 BOTTLE in 1 CARTON (25021-108-99) > 100 mL in 1 BOTTLE | 1 bottle | 2009-11-05 | 0000-00-00 | No | No | Current |