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SudoGest
SudoGest - 0904-5803-15 - (Pseudoephedrine Hydrochloride)
Drug Information of SudoGest
| Product NDC: | 0904-5803 |
| Proprietary Name: | SudoGest |
| Non Proprietary Name: | Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 120 mg/1 & nbsp; Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SudoGest
| Product NDC: | 0904-5803 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077442 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060428 |
Package Information of SudoGest
| Package NDC: | 0904-5803-15 |
| Package Description: | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5803-15) |
NDC Information of SudoGest
| NDC Code | 0904-5803-15 |
| Proprietary Name | SudoGest |
| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5803-15) |
| Product NDC | 0904-5803 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060428 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
