Ceftriaxone Sodium
- Product NDC
- 70518-2301
- 11-digit product format
- 705182301
- Labeler code
- 70518
- Product ID
- 70518-2301_e53238e3-7269-4e2e-e053-2995a90a8deb
- 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
- 2019-09-04
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2301 | CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250311_f33a15cb-2ec8-4a5b-84ff-362fe9a67128.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2301-0 | 70518230100 | 10 VIAL, SINGLE-USE in 1 CARTON (70518-2301-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2301-1) | 2019-09-04 | 0000-00-00 | No | No | Current |