Ampicillin and Sulbactam
- Product NDC
- 71288-006
- 11-digit product format
- 712880006
- Labeler code
- 71288
- Product ID
- 71288-006_0478d88f-efdc-479a-bd7d-b1f49e5de1e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin sodium and Sulbactam sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA090579
- Marketing category
- ANDA
- Marketing start
- 2022-01-17
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71288-006-30 | 71288000630 | 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-006-30) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (71288-006-31) | 2022-01-17 | 0000-00-00 | No | No | Current |