| NDC Code | 51662-1619-3 |
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| Package Description | 10 POUCH in 1 CASE (51662-1619-3) / 1 VIAL in 1 POUCH (51662-1619-2) / 20 mL in 1 VIAL |
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| Product NDC | 51662-1619 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Atropine Sulfate |
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| Non-Proprietary Name | Atropine Sulfate |
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| Dosage Form | INJECTION |
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| Usage | ENDOTRACHEAL; INTRAMEDULLARY; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20221001 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213561 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | ATROPINE SULFATE |
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| Strength | .4 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
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