| NDC Code | 70069-601-01 |
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| Package Description | 1 BOTTLE in 1 CARTON (70069-601-01) / 15 mL in 1 BOTTLE |
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| Product NDC | 70069-601 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Proparacaine Hydrochloride |
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| Non-Proprietary Name | Proparacaine Hydrochloride |
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| Dosage Form | SOLUTION/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20241010 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215816 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | PROPARACAINE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Local Anesthesia [PE], Local Anesthetic [EPC] |
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