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TYLENOL SINUS
TYLENOL SINUS - 50580-229-48 - (Acetaminophen and Phenylephrine hydrochloride)
Drug Information of TYLENOL SINUS
| Product NDC: | 50580-229 |
| Proprietary Name: | TYLENOL SINUS |
| Non Proprietary Name: | Acetaminophen and Phenylephrine hydrochloride |
| Active Ingredient(s): | 325; 5 mg/1; mg/1 & nbsp; Acetaminophen and Phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TYLENOL SINUS
| Product NDC: | 50580-229 |
| 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: | 20070701 |
Package Information of TYLENOL SINUS
| Package NDC: | 50580-229-48 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (50580-229-48) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Information of TYLENOL SINUS
| NDC Code | 50580-229-48 |
| Proprietary Name | TYLENOL SINUS |
| Package Description | 4 BLISTER PACK in 1 CARTON (50580-229-48) > 12 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 50580-229 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Phenylephrine hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
