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Childrens Silfedrine
Childrens Silfedrine - 54838-104-40 - (Pseudoephedrine hydrochloride)
Drug Information of Childrens Silfedrine
| Product NDC: | 54838-104 |
| Proprietary Name: | Childrens Silfedrine |
| Non Proprietary Name: | Pseudoephedrine hydrochloride |
| Active Ingredient(s): | 15 mg/5mL & nbsp; Pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Silfedrine
| Product NDC: | 54838-104 |
| Labeler Name: | Silarx Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010105 |
Package Information of Childrens Silfedrine
| Package NDC: | 54838-104-40 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (54838-104-40) |
NDC Information of Childrens Silfedrine
| NDC Code | 54838-104-40 |
| Proprietary Name | Childrens Silfedrine |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (54838-104-40) |
| Product NDC | 54838-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20010105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Silarx Pharmaceuticals, Inc |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
