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Non-Drowsy Nasal Decongestant
Non-Drowsy Nasal Decongestant - 59779-112-22 - (Pseudoephedrine HCl)
Drug Information of Non-Drowsy Nasal Decongestant
| Product NDC: | 59779-112 |
| Proprietary Name: | Non-Drowsy Nasal Decongestant |
| 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) |
Labeler Information of Non-Drowsy Nasal Decongestant
| Product NDC: | 59779-112 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19810825 |
Package Information of Non-Drowsy Nasal Decongestant
| Package NDC: | 59779-112-22 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-112-22) > 48 TABLET in 1 BLISTER PACK |
NDC Information of Non-Drowsy Nasal Decongestant
| NDC Code | 59779-112-22 |
| Proprietary Name | Non-Drowsy Nasal Decongestant |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-112-22) > 48 TABLET in 1 BLISTER PACK |
| Product NDC | 59779-112 |
| 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 | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
