| NDC Code | 0641-1398-35 |
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| Package Description | 25 AMPULE in 1 CARTON (0641-1398-35) / 2 mL in 1 AMPULE (0641-1398-31) |
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| Product NDC | 0641-1398 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Chlorpromazine Hydrochloride |
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| Non-Proprietary Name | Chlorpromazine Hydrochloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAMUSCULAR |
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| Start Marketing Date | 19740725 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA083329 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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