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Ampicillin
Ampicillin - 36000-071-10 - (Ampicillin sodium)
Drug Information of Ampicillin
| Product NDC: | 36000-071 |
| Proprietary Name: | Ampicillin |
| Non Proprietary Name: | Ampicillin sodium |
| Active Ingredient(s): | 500 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: | 36000-071 |
| Labeler Name: | Claris Lifesciences, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090354 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100425 |
Package Information of Ampicillin
| Package NDC: | 36000-071-10 |
| Package Description: | 10 VIAL in 1 CARTON (36000-071-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of Ampicillin
| NDC Code | 36000-071-10 |
| Proprietary Name | Ampicillin |
| Package Description | 10 VIAL in 1 CARTON (36000-071-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 36000-071 |
| 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 | 20100425 |
| Marketing Category Name | ANDA |
| Labeler Name | Claris Lifesciences, Inc. |
| Substance Name | AMPICILLIN SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
