| NDC Code | 52584-082-10 |
|---|
| Package Description | 1 VIAL in 1 BAG (52584-082-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
|---|
| Product NDC | 52584-082 |
|---|
| 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 | 20181010 |
|---|
| End Marketing Date | 20231031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065499 |
|---|
| Manufacturer | General Injectables and Vaccines, Inc. |
|---|
| Substance Name | AMPICILLIN SODIUM |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/1 |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
|---|