| NDC Code | 0703-2201-04 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0703-2201-04) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-2201-01) |
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| Product NDC | 0703-2201 |
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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, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20021001 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040454 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
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