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Mydfrin
Mydfrin - 0065-0342-03 - (phenylephrine hydrochloride)
Drug Information of Mydfrin
| Product NDC: | 0065-0342 |
| Proprietary Name: | Mydfrin |
| Non Proprietary Name: | phenylephrine hydrochloride |
| Active Ingredient(s): | 25 mg/mL & nbsp; phenylephrine hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mydfrin
| Product NDC: | 0065-0342 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19790215 |
Package Information of Mydfrin
| Package NDC: | 0065-0342-03 |
| Package Description: | 3 mL in 1 BOTTLE, DROPPER (0065-0342-03) |
NDC Information of Mydfrin
| NDC Code | 0065-0342-03 |
| Proprietary Name | Mydfrin |
| Package Description | 3 mL in 1 BOTTLE, DROPPER (0065-0342-03) |
| Product NDC | 0065-0342 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phenylephrine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19790215 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
