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Silafed
Silafed - 54838-101-40 - (Pseudoephedrine hydrochloride and Triprolidine hydrochloride)
Drug Information of Silafed
| Product NDC: | 54838-101 |
| Proprietary Name: | Silafed |
| Non Proprietary Name: | Pseudoephedrine hydrochloride and Triprolidine hydrochloride |
| Active Ingredient(s): | 30; 1.25 mg/5mL; mg/5mL & nbsp; Pseudoephedrine hydrochloride and Triprolidine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Silafed
| Product NDC: | 54838-101 |
| Labeler Name: | Silarx Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19881005 |
Package Information of Silafed
| Package NDC: | 54838-101-40 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (54838-101-40) |
NDC Information of Silafed
| NDC Code | 54838-101-40 |
| Proprietary Name | Silafed |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (54838-101-40) |
| Product NDC | 54838-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine hydrochloride and Triprolidine hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19881005 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Silarx Pharmaceuticals, Inc |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE |
| Strength Number | 30; 1.25 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
