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AMPICILLIN
AMPICILLIN - 52584-135-10 - (ampicillin sodium)
Drug Information of AMPICILLIN
| Product NDC: | 52584-135 |
| Proprietary Name: | AMPICILLIN |
| Non Proprietary Name: | ampicillin sodium |
| Active Ingredient(s): | 500 mg/500mg & 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: | 52584-135 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063146 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130313 |
Package Information of AMPICILLIN
| Package NDC: | 52584-135-10 |
| Package Description: | 1 VIAL in 1 BAG (52584-135-10) > 500 mg in 1 VIAL |
NDC Information of AMPICILLIN
| NDC Code | 52584-135-10 |
| Proprietary Name | AMPICILLIN |
| Package Description | 1 VIAL in 1 BAG (52584-135-10) > 500 mg in 1 VIAL |
| Product NDC | 52584-135 |
| 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 | 20130313 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | AMPICILLIN SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/500mg |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
