| NDC Code | 70069-371-25 |
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| Package Description | 25 VIAL in 1 CARTON (70069-371-25) / 2 mL in 1 VIAL (70069-371-01) |
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| Product NDC | 70069-371 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Prochlorperazine Edisylate |
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| Non-Proprietary Name | Prochlorperazine Edisylate |
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| Dosage Form | INJECTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20241010 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212257 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | PROCHLORPERAZINE EDISYLATE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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