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 |