Product NDC: | 42702-102 |
Proprietary Name: | Phenylephrine Hydrochloride |
Non Proprietary Name: | phenylephrine hydrochloride |
Active Ingredient(s): | 2.5 mg/mL & nbsp; phenylephrine hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42702-102 |
Labeler Name: | Paragon BioTeck, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA203510 |
Marketing Category: | NDA |
Start Marketing Date: | 20130415 |
Package NDC: | 42702-102-15 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (42702-102-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 42702-102-15 |
Proprietary Name | Phenylephrine Hydrochloride |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (42702-102-15) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 42702-102 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | phenylephrine hydrochloride |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130415 |
Marketing Category Name | NDA |
Labeler Name | Paragon BioTeck, Inc. |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |