ampicillin sodium and sulbactam sodium
- Product NDC
- 67457-649
- 11-digit product format
- 674570649
- Labeler code
- 67457
- Product ID
- 67457-649_ba79fbac-3d42-45d5-a9e8-08d9ba15018e
- 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
- ANDA202197
- Marketing category
- ANDA
- Marketing start
- 2014-04-08
- Marketing end
- 2023-12-31
- Substance
- AMPICILLIN SODIUM; SULBACTAM SODIUM
- Active strength
- 100 mg/mL; mg/mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-649-10 | 67457064910 | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (67457-649-10) > 92 mL in 1 VIAL, PHARMACY BULK PACKAGE | 2014-04-08 | 0000-00-00 | No | No | Current |