Ampicillin and Sulbactam
- Product NDC
- 0781-3033
- 11-digit product format
- 007813033
- Labeler code
- 0781
- Product ID
- 0781-3033_0ebf3cee-a9be-4ea6-9270-b8b840c85505
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin sodium and Sulbactam sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA065241
- Marketing category
- ANDA
- Marketing start
- 2006-07-25
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 0781-3033-95 | 00781303395 | 10 VIAL in 1 CARTON (0781-3033-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3033-70) | 10 vial | 2006-07-25 | 0000-00-00 | No | No | Current |