| NDC Code | 51662-1311-1 |
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| Package Description | 20 mL in 1 VIAL, MULTI-DOSE (51662-1311-1) |
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| Product NDC | 51662-1311 |
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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 | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20181006 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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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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