NDC Code | 70860-112-15 |
Package Description | 10 VIAL in 1 CARTON (70860-112-15) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70860-112-41) |
Product NDC | 70860-112 |
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 | 20180801 |
Marketing Category Name | ANDA |
Application Number | ANDA090354 |
Manufacturer | Athenex Pharmaceutical Division, LLC. |
Substance Name | AMPICILLIN SODIUM |
Strength | 250 |
Strength Unit | mg/1 |
Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |