NDC Code | 65219-014-10 |
Package Description | 10 VIAL in 1 CARTON (65219-014-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-014-01) |
Product NDC | 65219-014 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ampicillin |
Non-Proprietary Name | Ampicillin Sodium |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20191030 |
Marketing Category Name | ANDA |
Application Number | ANDA062719 |
Manufacturer | Fresenius Kabi USA, LLC |
Substance Name | AMPICILLIN SODIUM |
Strength | 250 |
Strength Unit | mg/1 |
Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |