| Product NDC: | 63629-1594 |
| Proprietary Name: | Phenylephrine Hydrochloride |
| 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) |
| Product NDC: | 63629-1594 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
| Package NDC: | 63629-1594-1 |
| Package Description: | 5 mL in 1 BOTTLE (63629-1594-1) |
| NDC Code | 63629-1594-1 |
| Proprietary Name | Phenylephrine Hydrochloride |
| Package Description | 5 mL in 1 BOTTLE (63629-1594-1) |
| Product NDC | 63629-1594 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |