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Ampicillin
Ampicillin - 0781-3402-95 - (Ampicillin sodium)
Drug Information of Ampicillin
| Product NDC: | 0781-3402 |
| 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: | 0781-3402 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA061395 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19710303 |
Package Information of Ampicillin
| Package NDC: | 0781-3402-95 |
| Package Description: | 10 VIAL, GLASS in 1 PACKAGE (0781-3402-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3402-78) |
NDC Information of Ampicillin
| NDC Code | 0781-3402-95 |
| Proprietary Name | Ampicillin |
| Package Description | 10 VIAL, GLASS in 1 PACKAGE (0781-3402-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3402-78) |
| Product NDC | 0781-3402 |
| 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 | 19710303 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | AMPICILLIN SODIUM |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
