Ceftriaxone
- Product NDC
- 66794-211
- 11-digit product format
- 667940211
- Labeler code
- 66794
- Product ID
- 66794-211_f092a251-81a4-ed5c-e053-2a95a90af949
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Piramal Critical Care Inc
- Application
- ANDA091049
- Marketing category
- ANDA
- Marketing start
- 2019-08-08
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 250 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66794-211-42 | 66794021142 | 25 VIAL in 1 CARTON (66794-211-42) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (66794-211-02) | 25 vial | 2019-08-08 | 0000-00-00 | No | No | Current |