Product NDC: | 55670-163 |
Proprietary Name: | MooreBrand Phenylephrine |
Non Proprietary Name: | PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 5 mg/1 & nbsp; PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55670-163 |
Labeler Name: | Moore Medical LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20081230 |
Package NDC: | 55670-163-13 |
Package Description: | 500 PACKET in 1 BOX, UNIT-DOSE (55670-163-13) > 2 TABLET, FILM COATED in 1 PACKET (55670-163-99) |
NDC Code | 55670-163-13 |
Proprietary Name | MooreBrand Phenylephrine |
Package Description | 500 PACKET in 1 BOX, UNIT-DOSE (55670-163-13) > 2 TABLET, FILM COATED in 1 PACKET (55670-163-99) |
Product NDC | 55670-163 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20081230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Moore Medical LLC |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |