| NDC Code | 51662-1595-3 |
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| Package Description | 10 POUCH in 1 CASE (51662-1595-3) / 1 VIAL in 1 POUCH (51662-1595-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
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| Product NDC | 51662-1595 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ampicillin |
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| Non-Proprietary Name | Ampicillin |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20220818 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA062719 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | AMPICILLIN SODIUM |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
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