Product NDC: | 63868-146 |
Proprietary Name: | Maximum Strength Suphedrine |
Non Proprietary Name: | Pseudoephedrine HCl |
Active Ingredient(s): | 30 mg/1 & nbsp; Pseudoephedrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63868-146 |
Labeler Name: | CHAIN DRUG MARKETING ASSOCIATION INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19810825 |
Package NDC: | 63868-146-24 |
Package Description: | 1 BLISTER PACK in 1 CARTON (63868-146-24) > 24 TABLET in 1 BLISTER PACK |
NDC Code | 63868-146-24 |
Proprietary Name | Maximum Strength Suphedrine |
Package Description | 1 BLISTER PACK in 1 CARTON (63868-146-24) > 24 TABLET in 1 BLISTER PACK |
Product NDC | 63868-146 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Pseudoephedrine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19810825 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CHAIN DRUG MARKETING ASSOCIATION INC |
Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes |