Ceftriaxone Sodium
- Product NDC
- 70518-0168
- 11-digit product format
- 705180168
- Labeler code
- 70518
- Product ID
- 70518-0168_df5c8405-d7ce-2b92-e053-2995a90ab7ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065169
- Marketing category
- ANDA
- Marketing start
- 2017-01-20
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0168-0 | 70518016800 | 10 VIAL, SINGLE-USE in 1 CARTON (70518-0168-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE | 2017-01-20 | 0000-00-00 | No | No | Current |