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SUDAFED
SUDAFED - 50580-545-24 - (Pseudoephedrine Hydrochloride)
Drug Information of SUDAFED
| Product NDC: | 50580-545 |
| Proprietary Name: | SUDAFED |
| Non Proprietary Name: | Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUDAFED
| Product NDC: | 50580-545 |
| 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: | 20111001 |
Package Information of SUDAFED
| Package NDC: | 50580-545-24 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (50580-545-24) > 8 TABLET, COATED in 1 BLISTER PACK |
NDC Information of SUDAFED
| NDC Code | 50580-545-24 |
| Proprietary Name | SUDAFED |
| Package Description | 3 BLISTER PACK in 1 CARTON (50580-545-24) > 8 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 50580-545 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
