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Proparacaine Hydrochloride
Proparacaine Hydrochloride - 17478-263-12 - (Proparacaine Hydrochloride)
Drug Information of Proparacaine Hydrochloride
| Product NDC: | 17478-263 |
| Proprietary Name: | Proparacaine Hydrochloride |
| Non Proprietary Name: | Proparacaine Hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; Proparacaine Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proparacaine Hydrochloride
| Product NDC: | 17478-263 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040277 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000316 |
Package Information of Proparacaine Hydrochloride
| Package NDC: | 17478-263-12 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-263-12) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of Proparacaine Hydrochloride
| NDC Code | 17478-263-12 |
| Proprietary Name | Proparacaine Hydrochloride |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-263-12) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-263 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Proparacaine Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20000316 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | PROPARACAINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Local Anesthesia [PE],Local Anesthetic [EPC] |
