ampicillin and sulbactam
- Product NDC
- 25021-186
- 11-digit product format
- 250210186
- Labeler code
- 25021
- Product ID
- 25021-186_d5ad5e18-0a8b-4977-9d6b-a5d423a55f3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin sodium and sulbactam sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA090579
- Marketing category
- ANDA
- Marketing start
- 2017-08-15
- Marketing end
- 2021-03-31
- Substance
- AMPICILLIN SODIUM; SULBACTAM SODIUM
- Active strength
- 1 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 |
|---|
| 25021-186-20 | 25021018620 | 10 VIAL in 1 CARTON (25021-186-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2017-08-15 | 0000-00-00 | No | No | Current |