ampicillin
- Product NDC
- 25021-134
- 11-digit product format
- 250210134
- Labeler code
- 25021
- Product ID
- 25021-134_de4361ab-e84b-43ff-9a85-24b0644edb9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA090354
- Marketing category
- ANDA
- Marketing start
- 2014-07-01
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 250 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 25021-134-10 | 25021013410 | 10 VIAL in 1 CARTON (25021-134-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2014-07-01 | 0000-00-00 | No | No | Current |