| 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 |