Home
>
National Drug Code (NDC)
>
Ampicillin
Ampicillin - 0069-0029-18 - (Ampicillin Sodium)
Drug Information of Ampicillin
| Product NDC: | 0069-0029 |
| 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: | 0069-0029 |
| Labeler Name: | Pfizer Laboratories, Division of Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065499 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100817 |
Package Information of Ampicillin
| Package NDC: | 0069-0029-18 |
| Package Description: | 10 VIAL in 1 BOX (0069-0029-18) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0069-0029-20) |
NDC Information of Ampicillin
| NDC Code | 0069-0029-18 |
| Proprietary Name | Ampicillin |
| Package Description | 10 VIAL in 1 BOX (0069-0029-18) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0069-0029-20) |
| Product NDC | 0069-0029 |
| 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 | 20100817 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Laboratories, Division of Pfizer Inc |
| Substance Name | AMPICILLIN SODIUM |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
