| NDC Code | 24208-740-02 |
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| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-740-02) > 5 mL in 1 BOTTLE, DROPPER |
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| Product NDC | 24208-740 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phenylephrine Hydrochloride |
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| Non-Proprietary Name | Phenylephrine Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 19900930 |
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| End Marketing Date | 20150131 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Bausch & Lomb Incorporated |
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| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | alpha-1 Adrenergic Agonist [EPC],Adrenergic alpha1-Agonists [MoA] |
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