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Sudafed
Sudafed - 50580-669-10 - (Pseudoephedrine Hydrochloride)
Drug Information of Sudafed
| Product NDC: | 50580-669 |
| Proprietary Name: | Sudafed |
| Non Proprietary Name: | Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 240 mg/1 & nbsp; Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sudafed
| Product NDC: | 50580-669 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020021 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081001 |
Package Information of Sudafed
| Package NDC: | 50580-669-10 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (50580-669-10) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Sudafed
| NDC Code | 50580-669-10 |
| Proprietary Name | Sudafed |
| Package Description | 2 BLISTER PACK in 1 CARTON (50580-669-10) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 50580-669 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20081001 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 240 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
