| NDC Code | 0143-9869-22 |
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| Package Description | 1 mL in 1 AMPULE (0143-9869-22) |
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| Product NDC | 0143-9869 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Promethazine Hydrochloride |
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| Non-Proprietary Name | Promethazine Hydrochloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20080424 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040737 |
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| Manufacturer | West-ward Pharmaceutical Corp |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
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