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SUDAFED PE Pressure PLUS Pain PLUS Mucus
SUDAFED PE Pressure PLUS Pain PLUS Mucus - 50580-680-25 - (Acetaminophen, Guaifenesin, and Phenylephrine hydrochloride)
Drug Information of SUDAFED PE Pressure PLUS Pain PLUS Mucus
| Product NDC: | 50580-680 |
| Proprietary Name: | SUDAFED PE Pressure PLUS Pain PLUS Mucus |
| Non Proprietary Name: | Acetaminophen, Guaifenesin, and Phenylephrine hydrochloride |
| Active Ingredient(s): | 325; 200; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Guaifenesin, and Phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUDAFED PE Pressure PLUS Pain PLUS Mucus
| Product NDC: | 50580-680 |
| Labeler Name: | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130701 |
Package Information of SUDAFED PE Pressure PLUS Pain PLUS Mucus
| Package NDC: | 50580-680-25 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (50580-680-25) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of SUDAFED PE Pressure PLUS Pain PLUS Mucus
| NDC Code | 50580-680-25 |
| Proprietary Name | SUDAFED PE Pressure PLUS Pain PLUS Mucus |
| Package Description | 2 BLISTER PACK in 1 CARTON (50580-680-25) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 50580-680 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Guaifenesin, and Phenylephrine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
