Ampicillin
- Product NDC
- 10515-772
- 11-digit product format
- 105150772
- Labeler code
- 10515
- Product ID
- 10515-772_9bc6017d-6f30-45d6-9a85-8d39c736d214
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- GC Hanford Manufacturing Company
- Application
- ANDA062772
- Marketing category
- ANDA
- Marketing start
- 2008-02-15
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 1 g/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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10515-772-00 | 10515077200 | 10 VIAL, GLASS in 1 TRAY (10515-772-00) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS | 2008-03-06 | 0000-00-00 | No | No | Current |