Ceftriaxone Sodium
- Product NDC
- 43858-632
- 11-digit product format
- 438580632
- Labeler code
- 43858
- Product ID
- 43858-632_8b6a3f9b-5e2f-48a1-a762-c9b9421975fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sandoz GmbH
- Application
- ANDA065169
- Marketing category
- ANDA
- Marketing start
- 2005-05-09
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43858-632-01 | 43858063201 | 10 VIAL, SINGLE-USE in 1 CARTON (43858-632-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2018-03-19 | 0000-00-00 | No | No | Current |