| NDC Code | 50436-1029-1 |
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| Package Description | 120 mL in 1 BOTTLE (50436-1029-1) |
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| Product NDC | 50436-1029 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Promethazine With Codeine |
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| Non-Proprietary Name | Promethazine Hydrochloride And Codeine Phosphate |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20060131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040650 |
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| Manufacturer | Unit Dose Services |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE; CODEINE PHOSPHATE |
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| Strength | 6.25; 10 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [CS],Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
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| DEA Schedule | CV |
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