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Alcaine
Alcaine - 0998-0016-15 - (proparacaine hydrochloride)
Drug Information of Alcaine
| Product NDC: | 0998-0016 |
| Proprietary Name: | Alcaine |
| Non Proprietary Name: | proparacaine hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; proparacaine hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alcaine
| Product NDC: | 0998-0016 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080027 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19731019 |
Package Information of Alcaine
| Package NDC: | 0998-0016-15 |
| Package Description: | 15 mL in 1 BOTTLE (0998-0016-15) |
NDC Information of Alcaine
| NDC Code | 0998-0016-15 |
| Proprietary Name | Alcaine |
| Package Description | 15 mL in 1 BOTTLE (0998-0016-15) |
| Product NDC | 0998-0016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | proparacaine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19731019 |
| Marketing Category Name | ANDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | PROPARACAINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Local Anesthesia [PE],Local Anesthetic [EPC] |
