Product NDC: | 41268-094 |
Proprietary Name: | nasal decongestant pe |
Non Proprietary Name: | Phenylephrine Hydrochloride |
Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41268-094 |
Labeler Name: | Hannaford Brothers Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20050908 |
Package NDC: | 41268-094-68 |
Package Description: | 2 BLISTER PACK in 1 CARTON (41268-094-68) > 18 TABLET in 1 BLISTER PACK |
NDC Code | 41268-094-68 |
Proprietary Name | nasal decongestant pe |
Package Description | 2 BLISTER PACK in 1 CARTON (41268-094-68) > 18 TABLET in 1 BLISTER PACK |
Product NDC | 41268-094 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Phenylephrine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20050908 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Hannaford Brothers Company |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |