ampicillin sodium and sulbactam sodium
- Product NDC
- 82449-900
- 11-digit product format
- 824490900
- Labeler code
- 82449
- Product ID
- 82449-900_d4e9ca57-ed59-c88e-e053-2995a90a9a78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin sodium and sulbactam sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Steriscience Specialties Private Limited
- Application
- ANDA201024
- Marketing category
- ANDA
- Marketing start
- 2014-04-08
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM; SULBACTAM SODIUM
- Active strength
- 1 g/1; g/1
- Pharmacologic classes
- beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA],Penicillin-class Antibacterial [EPC],Penicillins [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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82449-900-02 | 82449090002 | 10 VIAL in 1 CARTON (82449-900-02) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2017-12-01 | 0000-00-00 | No | No | Current |