ampicillin sodium and sulbactam sodium
- Product NDC
- 67457-349
- 11-digit product format
- 674570349
- Labeler code
- 67457
- Product ID
- 67457-349_8ebb4add-3890-49ef-b5c9-b03400c2a3d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin sodium and sulbactam sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA201024
- Marketing category
- ANDA
- Marketing start
- 2014-04-08
- Marketing end
- 2024-02-29
- Substance
- AMPICILLIN SODIUM; SULBACTAM SODIUM
- Active strength
- 2 g/1; g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 67457-349-10 | 67457034910 | 10 VIAL in 1 CARTON (67457-349-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2016-10-31 | 0000-00-00 | No | No | Current |