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Pseudoephedrine Plus
Pseudoephedrine Plus - 10267-1016-8 - (Pseudoephedrine Hydrochloride Chlorpherniamine Maleate)
Drug Information of Pseudoephedrine Plus
| Product NDC: | 10267-1016 |
| Proprietary Name: | Pseudoephedrine Plus |
| Non Proprietary Name: | Pseudoephedrine Hydrochloride Chlorpherniamine Maleate |
| Active Ingredient(s): | 4; 60 mg/1; mg/1 & nbsp; Pseudoephedrine Hydrochloride Chlorpherniamine Maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pseudoephedrine Plus
| Product NDC: | 10267-1016 |
| Labeler Name: | Contract Pharmacal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010220 |
Package Information of Pseudoephedrine Plus
| Package NDC: | 10267-1016-8 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (10267-1016-8) > 24 TABLET in 1 BLISTER PACK |
NDC Information of Pseudoephedrine Plus
| NDC Code | 10267-1016-8 |
| Proprietary Name | Pseudoephedrine Plus |
| Package Description | 1 BLISTER PACK in 1 CARTON (10267-1016-8) > 24 TABLET in 1 BLISTER PACK |
| Product NDC | 10267-1016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine Hydrochloride Chlorpherniamine Maleate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010220 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Contract Pharmacal Corp |
| Substance Name | CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 4; 60 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
