Ampicillin Sodium
- Product NDC
- 67457-404
- 11-digit product format
- 674570404
- Labeler code
- 67457
- Product ID
- 67457-404_02a590f3-e725-4fe0-a130-d5342ca6f759
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA202198
- Marketing category
- ANDA
- Marketing start
- 2016-09-12
- Marketing end
- 2023-09-30
- Substance
- AMPICILLIN SODIUM
- Active strength
- 10 g/100mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- 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 |
|---|
| 67457-404-10 | 67457040410 | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (67457-404-10) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE | 2016-09-12 | 2023-09-30 | No | No | Current |