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Ampicillin
Ampicillin - 55150-111-10 - (Ampicillin Sodium)
Drug Information of Ampicillin
| Product NDC: | 55150-111 |
| Proprietary Name: | Ampicillin |
| Non Proprietary Name: | Ampicillin Sodium |
| Active Ingredient(s): | 250 mg/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: | 55150-111 |
| Labeler Name: | AuroMedics Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065499 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120201 |
Package Information of Ampicillin
| Package NDC: | 55150-111-10 |
| Package Description: | 10 VIAL in 1 BOX (55150-111-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of Ampicillin
| NDC Code | 55150-111-10 |
| Proprietary Name | Ampicillin |
| Package Description | 10 VIAL in 1 BOX (55150-111-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 55150-111 |
| 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 | 20120201 |
| Marketing Category Name | ANDA |
| Labeler Name | AuroMedics Pharma LLC |
| Substance Name | AMPICILLIN SODIUM |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
