Home
>
National Drug Code (NDC)
>
Ampicillin
Ampicillin - 10515-772-00 - (Ampicillin Sodium)
Drug Information of Ampicillin
| Product NDC: | 10515-772 |
| Proprietary Name: | Ampicillin |
| Non Proprietary Name: | Ampicillin Sodium |
| Active Ingredient(s): | 1 g/1 & nbsp; Ampicillin Sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ampicillin
| Product NDC: | 10515-772 |
| Labeler Name: | GC Hanford Manufacturing Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062772 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080215 |
Package Information of Ampicillin
| Package NDC: | 10515-772-00 |
| Package Description: | 10 VIAL, GLASS in 1 TRAY (10515-772-00) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS |
NDC Information of Ampicillin
| NDC Code | 10515-772-00 |
| Proprietary Name | Ampicillin |
| Package Description | 10 VIAL, GLASS in 1 TRAY (10515-772-00) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS |
| Product NDC | 10515-772 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ampicillin Sodium |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20080215 |
| Marketing Category Name | ANDA |
| Labeler Name | GC Hanford Manufacturing Company |
| Substance Name | AMPICILLIN SODIUM |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
