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Suphedrine
Suphedrine - 11822-0054-6 - (Pseudoephedrine Hydrochloride)
Drug Information of Suphedrine
| Product NDC: | 11822-0054 |
| Proprietary Name: | Suphedrine |
| 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 Suphedrine
| Product NDC: | 11822-0054 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075153 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020813 |
Package Information of Suphedrine
| Package NDC: | 11822-0054-6 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (11822-0054-6) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Suphedrine
| NDC Code | 11822-0054-6 |
| Proprietary Name | Suphedrine |
| Package Description | 2 BLISTER PACK in 1 CARTON (11822-0054-6) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 11822-0054 |
| 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 | 20020813 |
| Marketing Category Name | ANDA |
| Labeler Name | Rite Aid Corporation |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
